Skip to main content
Erschienen in: Pediatric Surgery International 2/2019

01.11.2018 | Original Article

Consanguinity and its relevance for the incidence of megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): systematic review

verfasst von: Hiroki Nakamura, Anne Marie O’Donnell, Prem Puri

Erschienen in: Pediatric Surgery International | Ausgabe 2/2019

Einloggen, um Zugang zu erhalten

Abstract

Background/purpose

Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital and generally fatal cause of functional intestinal obstruction in the newborn. The cause of this syndrome is unknown. Familial occurrence and reports of consanguinity in MMIHS implies that genetic factors may have an important role in the pathogenesis of this syndrome. The aim of the study was to determine the consequence of consanguinity for the incidence of MMIHS.

Methods

A literature search was performed using the keywords “megacystis microcolon intestinal hypoperistalsis” for studies published between 1976 and 2018. Retrieved articles, including additional studies from reference lists, were reviewed for consanguinity between parents and recurrence of MMIHS between siblings. Data were extracted for cases where familial MMIHS was present.

Results

A total of 450 patients with the diagnosis of MMIHS have been reported in the literature. There were 56 (12%) cases in which familial MMIHS was confirmed, 25 families with multiple siblings and 3 families with single affected infant. Of the 25 families with multiple siblings, 22 families had 2 siblings with confirmed MMIHS and 3 families had 3 children each with MMIHS. Consanguinity between parents was confirmed in 30 cases (18 siblings and 12 individual cases). Female-to-male ratio in the 30 patients was 4.4:1.

Conclusion

The occurrence of MMIHS in the offspring of consanguineous parents and recurrence in siblings of healthy parents suggest that MMIHS is an autosomal recessive disorder. Pre-marital and pre-conception counselling of consanguineous populations is recommended to prevent harmful consequences.
Literatur
1.
Zurück zum Zitat Puri P, Shinkai M (2005) Megacystis microcolon intestinal hypoperistalsis syndrome. Semin Pediatr Surg 14:58–63CrossRefPubMed Puri P, Shinkai M (2005) Megacystis microcolon intestinal hypoperistalsis syndrome. Semin Pediatr Surg 14:58–63CrossRefPubMed
2.
Zurück zum Zitat Berdon WE, Baker DH, Blanc WA, Gay B, Santulli TV, Donovan C (1976) Megacystis-microcolon-intestinal hypoperistalsis syndrome: a new cause of intestinal obstruction in the newborn. Report of radiologic findings in five newborn girls. AJR Am J Roentgenol 126:957–964CrossRefPubMed Berdon WE, Baker DH, Blanc WA, Gay B, Santulli TV, Donovan C (1976) Megacystis-microcolon-intestinal hypoperistalsis syndrome: a new cause of intestinal obstruction in the newborn. Report of radiologic findings in five newborn girls. AJR Am J Roentgenol 126:957–964CrossRefPubMed
3.
Zurück zum Zitat Andres AM, Miguel M, De la Torre C, Barrena S, Ramirez M, Hernandez F et al (2010) Chronic idiopathic intestinal pseudoobstruction and Berdon syndrome: still a diagnostic and therapeutic challenge for the pediatric surgeon. Cir Pediatr 23:215–221PubMed Andres AM, Miguel M, De la Torre C, Barrena S, Ramirez M, Hernandez F et al (2010) Chronic idiopathic intestinal pseudoobstruction and Berdon syndrome: still a diagnostic and therapeutic challenge for the pediatric surgeon. Cir Pediatr 23:215–221PubMed
4.
Zurück zum Zitat Kohler M, Pease PW, Upadhyay V (2004) Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) in siblings: case report and review of the literature. Eur J Pediatr Surg 14:362–367CrossRefPubMed Kohler M, Pease PW, Upadhyay V (2004) Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) in siblings: case report and review of the literature. Eur J Pediatr Surg 14:362–367CrossRefPubMed
5.
Zurück zum Zitat Halim D, Wilson MP, Oliver D, Brosens E, Verheij JB, Han Y et al (2017) Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice. Proc Natl Acad Sci USA 114:E2739–E2747CrossRefPubMed Halim D, Wilson MP, Oliver D, Brosens E, Verheij JB, Han Y et al (2017) Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice. Proc Natl Acad Sci USA 114:E2739–E2747CrossRefPubMed
6.
Zurück zum Zitat Halim D, Hofstra RM, Signorile L, Verdijk RM, van der Werf CS, Sribudiani Y et al (2016) ACTG2 variants impair actin polymerization in sporadic megacystis microcolon intestinal hypoperistalsis syndrome. Hum Mol Genet 25:571–583CrossRefPubMed Halim D, Hofstra RM, Signorile L, Verdijk RM, van der Werf CS, Sribudiani Y et al (2016) ACTG2 variants impair actin polymerization in sporadic megacystis microcolon intestinal hypoperistalsis syndrome. Hum Mol Genet 25:571–583CrossRefPubMed
7.
Zurück zum Zitat Halim D, Brosens E, Muller F, Wangler MF, Beaudet AL, Lupski JR et al (2017) Loss-of-function variants in MYLK cause recessive megacystis microcolon intestinal hypoperistalsis syndrome. Am J Hum Genet 101:123–129CrossRefPubMedPubMedCentral Halim D, Brosens E, Muller F, Wangler MF, Beaudet AL, Lupski JR et al (2017) Loss-of-function variants in MYLK cause recessive megacystis microcolon intestinal hypoperistalsis syndrome. Am J Hum Genet 101:123–129CrossRefPubMedPubMedCentral
8.
Zurück zum Zitat Korğalı E, Yavuz A, Şimşek CEÇ, Güney C, Kurtulgan HK, Başer B et al (2018) Megacystis microcolon intestinal hypoperistalsis syndrome in which a different de novo Actg2 gene mutation was detected: a case report. Fetal Pediatric Pathol 37:109–116CrossRef Korğalı E, Yavuz A, Şimşek CEÇ, Güney C, Kurtulgan HK, Başer B et al (2018) Megacystis microcolon intestinal hypoperistalsis syndrome in which a different de novo Actg2 gene mutation was detected: a case report. Fetal Pediatric Pathol 37:109–116CrossRef
9.
Zurück zum Zitat Taguchi T, Ikeda K, Shono T, Goto S, Kubota M, Kawana T et al (1989) Autonomic innervation of the intestine from a baby with megacystis microcolon intestinal hypoperistalsis syndrome: I. Immunohistochemical study. J Pediatr Surg 24:1264–1266CrossRefPubMed Taguchi T, Ikeda K, Shono T, Goto S, Kubota M, Kawana T et al (1989) Autonomic innervation of the intestine from a baby with megacystis microcolon intestinal hypoperistalsis syndrome: I. Immunohistochemical study. J Pediatr Surg 24:1264–1266CrossRefPubMed
10.
Zurück zum Zitat Kubota M, Ikeda K, Ito Y (1989) Autonomic innervation of the intestine from a baby with megacystis microcolon intestinal hypoperistalsis syndrome: II. Electrophysiological study. J Pediatr Surg 24:1267–1270CrossRefPubMed Kubota M, Ikeda K, Ito Y (1989) Autonomic innervation of the intestine from a baby with megacystis microcolon intestinal hypoperistalsis syndrome: II. Electrophysiological study. J Pediatr Surg 24:1267–1270CrossRefPubMed
11.
Zurück zum Zitat Granata C, Puri P (1997) Megacystis-microcolon-intestinal hypoperistalsis syndrome. J Pediatr Gastroenterol Nutr 25:12–19CrossRefPubMed Granata C, Puri P (1997) Megacystis-microcolon-intestinal hypoperistalsis syndrome. J Pediatr Gastroenterol Nutr 25:12–19CrossRefPubMed
12.
Zurück zum Zitat Puri P, Lake BD, Gorman F, O’Donnell B, Nixon HH (1983) Megacystis-microcolon-intestinal hypoperistalsis syndrome: a visceral myopathy. J Pediatr Surg 18:64–69CrossRefPubMed Puri P, Lake BD, Gorman F, O’Donnell B, Nixon HH (1983) Megacystis-microcolon-intestinal hypoperistalsis syndrome: a visceral myopathy. J Pediatr Surg 18:64–69CrossRefPubMed
13.
Zurück zum Zitat Ciftci AO, Cook RC, van Velzen D (1996) Megacystis microcolon intestinal hypoperistalsis syndrome: evidence of a primary myocellular defect of contractile fiber synthesis. J Pediatr Surg 31:1706–1711CrossRefPubMed Ciftci AO, Cook RC, van Velzen D (1996) Megacystis microcolon intestinal hypoperistalsis syndrome: evidence of a primary myocellular defect of contractile fiber synthesis. J Pediatr Surg 31:1706–1711CrossRefPubMed
14.
Zurück zum Zitat Rolle U, O’Briain S, Pearl RH, Puri P (2002) Megacystis-microcolon-intestinal hypoperistalsis syndrome: evidence of intestinal myopathy. Pediatr Surg Int 18:2–5CrossRefPubMed Rolle U, O’Briain S, Pearl RH, Puri P (2002) Megacystis-microcolon-intestinal hypoperistalsis syndrome: evidence of intestinal myopathy. Pediatr Surg Int 18:2–5CrossRefPubMed
15.
Zurück zum Zitat Piotrowska AP, Rolle U, Chertin B, De Caluwe D, Bianchi A, Puri P (2003) Alterations in smooth muscle contractile and cytoskeleton proteins and interstitial cells of Cajal in megacystis microcolon intestinal hypoperistalsis syndrome. J Pediatr Surg 38:749–755CrossRefPubMed Piotrowska AP, Rolle U, Chertin B, De Caluwe D, Bianchi A, Puri P (2003) Alterations in smooth muscle contractile and cytoskeleton proteins and interstitial cells of Cajal in megacystis microcolon intestinal hypoperistalsis syndrome. J Pediatr Surg 38:749–755CrossRefPubMed
16.
Zurück zum Zitat Jona JZ, Werlin SL (1981) The megacystis microcolon intestinal hypoperistalsis syndrome: report of a case. J Pediatr Surg 16:749–751CrossRefPubMed Jona JZ, Werlin SL (1981) The megacystis microcolon intestinal hypoperistalsis syndrome: report of a case. J Pediatr Surg 16:749–751CrossRefPubMed
17.
Zurück zum Zitat Mc Laughlin D, Puri P (2013) Familial megacystis microcolon intestinal hypoperistalsis syndrome: a systematic review. Pediatr Surg Int 29:947–951CrossRefPubMed Mc Laughlin D, Puri P (2013) Familial megacystis microcolon intestinal hypoperistalsis syndrome: a systematic review. Pediatr Surg Int 29:947–951CrossRefPubMed
18.
Zurück zum Zitat Raofi V, Beatty E, Testa G, Abcarian H, Oberholzer J, Sankary H et al (2008) Combined living-related segmental liver and bowel transplantation for megacystis-microcolon-intestinal hypoperistalsis syndrome. J Pediatr Surg 43:e9–e11CrossRefPubMed Raofi V, Beatty E, Testa G, Abcarian H, Oberholzer J, Sankary H et al (2008) Combined living-related segmental liver and bowel transplantation for megacystis-microcolon-intestinal hypoperistalsis syndrome. J Pediatr Surg 43:e9–e11CrossRefPubMed
19.
Zurück zum Zitat Loinaz C, Rodriguez MM, Kato T, Mittal N, Romaguera RL, Bruce JH et al (2005) Intestinal and multivisceral transplantation in children with severe gastrointestinal dysmotility. J Pediatr Surg 40:1598–1604CrossRefPubMed Loinaz C, Rodriguez MM, Kato T, Mittal N, Romaguera RL, Bruce JH et al (2005) Intestinal and multivisceral transplantation in children with severe gastrointestinal dysmotility. J Pediatr Surg 40:1598–1604CrossRefPubMed
20.
Zurück zum Zitat Boman F, Sfeir R, Bonnevalle M, Besson R, Gottrand F, Jaubert F (2006) Complexity of pathological interpretation in megacystis-microcolon-intestinal hypoperistalsis syndrome. Ann Pathol 26:115–121CrossRefPubMed Boman F, Sfeir R, Bonnevalle M, Besson R, Gottrand F, Jaubert F (2006) Complexity of pathological interpretation in megacystis-microcolon-intestinal hypoperistalsis syndrome. Ann Pathol 26:115–121CrossRefPubMed
21.
Zurück zum Zitat Bornstein E, Atkins K, Fishman S, Monteagudo A, Bajor-Dattilo EB, Arif F et al (2008) Severe uropathy and normal amniotic fluid volume in a male fetus: sonographic surveillance leading to the diagnosis of megacystis-microcolon-intestinal hypoperistalsis syndrome. J Ultrasound Med 27:1099–1104CrossRefPubMed Bornstein E, Atkins K, Fishman S, Monteagudo A, Bajor-Dattilo EB, Arif F et al (2008) Severe uropathy and normal amniotic fluid volume in a male fetus: sonographic surveillance leading to the diagnosis of megacystis-microcolon-intestinal hypoperistalsis syndrome. J Ultrasound Med 27:1099–1104CrossRefPubMed
22.
Zurück zum Zitat El Fekih C, Ouerdiane N, Mourali M, Oueslati S, Oueslati B, Binous N et al (2009) Prenatal diagnosis and management of fetal megacystis. Tunis Med 87:887–890PubMed El Fekih C, Ouerdiane N, Mourali M, Oueslati S, Oueslati B, Binous N et al (2009) Prenatal diagnosis and management of fetal megacystis. Tunis Med 87:887–890PubMed
23.
Zurück zum Zitat Garel C, Dreux S, Philippe-Chomette P, Vuillard E, Oury JF, Muller F (2006) Contribution of fetal magnetic resonance imaging and amniotic fluid digestive enzyme assays to the evaluation of gastrointestinal tract abnormalities. Ultrasound Obstet Gynecol 28:282–291CrossRefPubMed Garel C, Dreux S, Philippe-Chomette P, Vuillard E, Oury JF, Muller F (2006) Contribution of fetal magnetic resonance imaging and amniotic fluid digestive enzyme assays to the evaluation of gastrointestinal tract abnormalities. Ultrasound Obstet Gynecol 28:282–291CrossRefPubMed
24.
Zurück zum Zitat Hidaka N, Kawamata K, Chiba Y (2006) Megacystis-microcolon-intestinal hypoperistalsis syndrome: in utero sonographic appearance and the contribution of vesicocentesis in antenatal diagnosis. J Ultrasound Med 25:765–769CrossRefPubMed Hidaka N, Kawamata K, Chiba Y (2006) Megacystis-microcolon-intestinal hypoperistalsis syndrome: in utero sonographic appearance and the contribution of vesicocentesis in antenatal diagnosis. J Ultrasound Med 25:765–769CrossRefPubMed
25.
Zurück zum Zitat Levin TL, Soghier L, Blitman NM, Vega-Rich C, Nafday S (2004) Megacystis-microcolon-intestinal hypoperistalsis and prune belly: overlapping syndromes. Pediatr Radiol 34:995–998CrossRefPubMed Levin TL, Soghier L, Blitman NM, Vega-Rich C, Nafday S (2004) Megacystis-microcolon-intestinal hypoperistalsis and prune belly: overlapping syndromes. Pediatr Radiol 34:995–998CrossRefPubMed
26.
Zurück zum Zitat Magana Pintiado MI, Al-Kassam Martinez M, Bousono Garcia C, Ramos Polo E, Gomez Alvarez ME (2008) The megacystis-microcolon-intestinal hypoperistalsis syndrome: apropos of a case with prolonged survival. Nutr Hosp 23:513–515PubMed Magana Pintiado MI, Al-Kassam Martinez M, Bousono Garcia C, Ramos Polo E, Gomez Alvarez ME (2008) The megacystis-microcolon-intestinal hypoperistalsis syndrome: apropos of a case with prolonged survival. Nutr Hosp 23:513–515PubMed
27.
Zurück zum Zitat Manop J, Chamnanvanakij S, Wattanasarn C (2004) Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): a case report in Thailand. J Med Assoc Thai 87:1385–1388PubMed Manop J, Chamnanvanakij S, Wattanasarn C (2004) Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): a case report in Thailand. J Med Assoc Thai 87:1385–1388PubMed
28.
Zurück zum Zitat Melek M, Edirne Y, Beger B, Cetin M (2009) Megacystis-microcolon-intestinal hypoperistalsis syndrome: a case report. Gastroenterol Res Pract 2009:282753CrossRefPubMedPubMedCentral Melek M, Edirne Y, Beger B, Cetin M (2009) Megacystis-microcolon-intestinal hypoperistalsis syndrome: a case report. Gastroenterol Res Pract 2009:282753CrossRefPubMedPubMedCentral
29.
Zurück zum Zitat Muller F, Dreux S, Vaast P, Dumez Y, Nisand I, Ville Y et al (2005) Prenatal diagnosis of megacystis-microcolon-intestinal hypoperistalsis syndrome: contribution of amniotic fluid digestive enzyme assay and fetal urinalysis. Prenat Diagn 25:203–209CrossRefPubMed Muller F, Dreux S, Vaast P, Dumez Y, Nisand I, Ville Y et al (2005) Prenatal diagnosis of megacystis-microcolon-intestinal hypoperistalsis syndrome: contribution of amniotic fluid digestive enzyme assay and fetal urinalysis. Prenat Diagn 25:203–209CrossRefPubMed
30.
Zurück zum Zitat Munch EM, Cisek LJ Jr, Roth DR (2009) Magnetic resonance imaging for prenatal diagnosis of multisystem disease: megacystis microcolon intestinal hypoperistalsis syndrome. Urology 74:592–594CrossRefPubMed Munch EM, Cisek LJ Jr, Roth DR (2009) Magnetic resonance imaging for prenatal diagnosis of multisystem disease: megacystis microcolon intestinal hypoperistalsis syndrome. Urology 74:592–594CrossRefPubMed
31.
Zurück zum Zitat Narayanan M, Murphy MS, Ainsworth JR, Arul GS (2007) Mydriasis in association with MMIHS in a female infant: evidence for involvement of the neuronal nicotinic acetylcholine receptor. J Pediatr Surg 42:1288–1290CrossRefPubMed Narayanan M, Murphy MS, Ainsworth JR, Arul GS (2007) Mydriasis in association with MMIHS in a female infant: evidence for involvement of the neuronal nicotinic acetylcholine receptor. J Pediatr Surg 42:1288–1290CrossRefPubMed
32.
Zurück zum Zitat Nathan JD, Rudolph JA, Kocoshis SA, Alonso MH, Ryckman FC, Tiao GM (2007) Isolated liver and multivisceral transplantation for total parenteral nutrition-related end-stage liver disease. J Pediatr Surg 42:143–147CrossRefPubMed Nathan JD, Rudolph JA, Kocoshis SA, Alonso MH, Ryckman FC, Tiao GM (2007) Isolated liver and multivisceral transplantation for total parenteral nutrition-related end-stage liver disease. J Pediatr Surg 42:143–147CrossRefPubMed
33.
Zurück zum Zitat Oka Y, Asabe K, Shirakusa T, Nabeshima K (2008) An antenatal appearance of megacystis-microcolon-intestinal hypoperistalsis syndrome. Turk J Pediatr 50:269–274PubMed Oka Y, Asabe K, Shirakusa T, Nabeshima K (2008) An antenatal appearance of megacystis-microcolon-intestinal hypoperistalsis syndrome. Turk J Pediatr 50:269–274PubMed
34.
Zurück zum Zitat Pohl J, Chandra R, Corpuz G, McNeal C, Macfarlane R (2008) Hypertriglyceridemia and megacystis-microcolon-intestinal hypoperistalsis syndrome. J Pediatr Gastroenterol Nutr 47:507–513CrossRefPubMed Pohl J, Chandra R, Corpuz G, McNeal C, Macfarlane R (2008) Hypertriglyceridemia and megacystis-microcolon-intestinal hypoperistalsis syndrome. J Pediatr Gastroenterol Nutr 47:507–513CrossRefPubMed
35.
Zurück zum Zitat Ruano R, Yoshisaki CT, Salustiano EM, Giron AM, Srougi M, Zugaib M (2011) Early fetal cystoscopy for first-trimester severe megacystis. Ultrasound Obstet Gynecol 37:696–701CrossRefPubMed Ruano R, Yoshisaki CT, Salustiano EM, Giron AM, Srougi M, Zugaib M (2011) Early fetal cystoscopy for first-trimester severe megacystis. Ultrasound Obstet Gynecol 37:696–701CrossRefPubMed
36.
Zurück zum Zitat Szigeti R, Chumpitazi BP, Finegold MJ, Ranganathan S, Craigen WJ, Carter BA et al (2010) Absent smooth muscle actin immunoreactivity of the small bowel muscularis propria circular layer in association with chromosome 15q11 deletion in megacystis-microcolon-intestinal hypoperistalsis syndrome. Pediatr Dev Pathol 13:322–325CrossRefPubMed Szigeti R, Chumpitazi BP, Finegold MJ, Ranganathan S, Craigen WJ, Carter BA et al (2010) Absent smooth muscle actin immunoreactivity of the small bowel muscularis propria circular layer in association with chromosome 15q11 deletion in megacystis-microcolon-intestinal hypoperistalsis syndrome. Pediatr Dev Pathol 13:322–325CrossRefPubMed
37.
Zurück zum Zitat Talisetti A, Longacre T, Pai RK, Kerner J (2009) Diversion colitis in a 19-year-old female with megacystis-microcolon-intestinal hypoperistalsis syndrome. Dig Dis Sci 54:2338–2340CrossRefPubMed Talisetti A, Longacre T, Pai RK, Kerner J (2009) Diversion colitis in a 19-year-old female with megacystis-microcolon-intestinal hypoperistalsis syndrome. Dig Dis Sci 54:2338–2340CrossRefPubMed
38.
Zurück zum Zitat Trebicka J, Biecker E, Gruenhage F, Stolte M, Meier-Ruge WA, Sauerbruch T et al (2008) Diagnosis of megacystis-microcolon intestinal hypoperistalsis syndrome with aplastic desmosis in adulthood: a case report. Eur J Gastroenterol Hepatol 20:353–355CrossRefPubMed Trebicka J, Biecker E, Gruenhage F, Stolte M, Meier-Ruge WA, Sauerbruch T et al (2008) Diagnosis of megacystis-microcolon intestinal hypoperistalsis syndrome with aplastic desmosis in adulthood: a case report. Eur J Gastroenterol Hepatol 20:353–355CrossRefPubMed
39.
Zurück zum Zitat Verbruggen SC, Wijnen RM, van den Berg P (2004) Megacystis-microcolon-intestinal hypoperistalsis syndrome: a case report. J Matern Fetal Neonatal Med 16:140–141CrossRefPubMed Verbruggen SC, Wijnen RM, van den Berg P (2004) Megacystis-microcolon-intestinal hypoperistalsis syndrome: a case report. J Matern Fetal Neonatal Med 16:140–141CrossRefPubMed
40.
Zurück zum Zitat Gosemann JH, Puri P (2011) Megacystis microcolon intestinal hypoperistalsis syndrome: systematic review of outcome. Pediatr Surg Int 27:1041–1046CrossRefPubMed Gosemann JH, Puri P (2011) Megacystis microcolon intestinal hypoperistalsis syndrome: systematic review of outcome. Pediatr Surg Int 27:1041–1046CrossRefPubMed
41.
Zurück zum Zitat Ravenscroft G, Pannell S, O’Grady G, Ong R, Ee HC, Faiz F et al (2018) Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstruction. Neurogastroenterol Motil 30(9):e13371CrossRefPubMed Ravenscroft G, Pannell S, O’Grady G, Ong R, Ee HC, Faiz F et al (2018) Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo-obstruction. Neurogastroenterol Motil 30(9):e13371CrossRefPubMed
42.
Zurück zum Zitat Hugar LA, Chaudhry R, Fuller TW, Cannon GM, Schneck FX, Ost MC et al (2018) Urologic phenotype and patterns of care in patients with megacystis microcolon intestinal hypoperistalsis syndrome presenting to a major pediatric transplantation center. Urology 119:127–132CrossRefPubMed Hugar LA, Chaudhry R, Fuller TW, Cannon GM, Schneck FX, Ost MC et al (2018) Urologic phenotype and patterns of care in patients with megacystis microcolon intestinal hypoperistalsis syndrome presenting to a major pediatric transplantation center. Urology 119:127–132CrossRefPubMed
43.
Zurück zum Zitat Buinoiu N, Panaitescu A, Demetrian M, Ionescu S, Peltecu G, Veduta A (2018) Ultrasound prenatal diagnosis of typical megacystis, microcolon, intestinal hypoperistalsis syndrome. Clin Case Rep 6:855–858CrossRefPubMedPubMedCentral Buinoiu N, Panaitescu A, Demetrian M, Ionescu S, Peltecu G, Veduta A (2018) Ultrasound prenatal diagnosis of typical megacystis, microcolon, intestinal hypoperistalsis syndrome. Clin Case Rep 6:855–858CrossRefPubMedPubMedCentral
44.
Zurück zum Zitat Whittington JR, Poole AT, Dutta EH, Munn MB (2017) A novel mutation in ACTG2 gene in mother with chronic intestinal pseudoobstruction and fetus with megacystis microcolon intestinal hypoperistalsis syndrome. Case Rep Genet 2017:9146507PubMedPubMedCentral Whittington JR, Poole AT, Dutta EH, Munn MB (2017) A novel mutation in ACTG2 gene in mother with chronic intestinal pseudoobstruction and fetus with megacystis microcolon intestinal hypoperistalsis syndrome. Case Rep Genet 2017:9146507PubMedPubMedCentral
45.
Zurück zum Zitat Pena J, Quinn KH, Jorizzo JR, Nitsche JF, Denney JM (2018) Megacystis-microcolon-intestinal hypoperistalsis syndrome: an unusual in utero presentation. J Ultrasound Med 37:1283–1286CrossRefPubMed Pena J, Quinn KH, Jorizzo JR, Nitsche JF, Denney JM (2018) Megacystis-microcolon-intestinal hypoperistalsis syndrome: an unusual in utero presentation. J Ultrasound Med 37:1283–1286CrossRefPubMed
46.
Zurück zum Zitat Velez-Perez A, Younes P, Tatevian N (2017) Placental fetal thrombotic vasculopathy occurring in association with megacystis-microcolon-intestinal hypoperistalsis syndrome: a case report. Ann Clin Lab Sci 47:357–361PubMed Velez-Perez A, Younes P, Tatevian N (2017) Placental fetal thrombotic vasculopathy occurring in association with megacystis-microcolon-intestinal hypoperistalsis syndrome: a case report. Ann Clin Lab Sci 47:357–361PubMed
47.
Zurück zum Zitat Pandav N, Gupta D, Ingle M, Sawant P (2015) Megacystic microcolon intestinal hypoperistalsis syndrome with mydriasis in a male child. Trop Gastroenterol 36:211–212CrossRefPubMed Pandav N, Gupta D, Ingle M, Sawant P (2015) Megacystic microcolon intestinal hypoperistalsis syndrome with mydriasis in a male child. Trop Gastroenterol 36:211–212CrossRefPubMed
48.
Zurück zum Zitat Moreno CA, Metze K, Lomazi EA, Bertola DR, Barbosa RH, Cosentino V et al (2016) Visceral myopathy: clinical and molecular survey of a cohort of seven new patients and state of the art of overlapping phenotypes. Am J Med Genet A 170:2965–2974CrossRefPubMedPubMedCentral Moreno CA, Metze K, Lomazi EA, Bertola DR, Barbosa RH, Cosentino V et al (2016) Visceral myopathy: clinical and molecular survey of a cohort of seven new patients and state of the art of overlapping phenotypes. Am J Med Genet A 170:2965–2974CrossRefPubMedPubMedCentral
49.
Zurück zum Zitat Wymer KM, Anderson BB, Wilkens AA, Gundeti MS (2016) Megacystis microcolon intestinal hypoperistalsis syndrome: case series and updated review of the literature with an emphasis on urologic management. J Pediatr Surg 51:1565–1573CrossRefPubMed Wymer KM, Anderson BB, Wilkens AA, Gundeti MS (2016) Megacystis microcolon intestinal hypoperistalsis syndrome: case series and updated review of the literature with an emphasis on urologic management. J Pediatr Surg 51:1565–1573CrossRefPubMed
50.
Zurück zum Zitat Okada M, Sato M, Ogura M, Kamei K, Matsuoka K, Ito S (2016) Central venous catheter infection-related glomerulonephritis under long-term parenteral nutrition: a report of two cases. BMC Res Notes 9:196CrossRefPubMedPubMedCentral Okada M, Sato M, Ogura M, Kamei K, Matsuoka K, Ito S (2016) Central venous catheter infection-related glomerulonephritis under long-term parenteral nutrition: a report of two cases. BMC Res Notes 9:196CrossRefPubMedPubMedCentral
51.
Zurück zum Zitat Lu W, Xiao Y, Huang J, Tao Y, Yan W, Lu L et al (2016) Mutation in actin gamma-2 responsible for megacystis microcolon intestinal hypoperistalsis syndrome in 4 chinese patients. J Pediatr Gastroenterol Nutr 63:624–626CrossRefPubMed Lu W, Xiao Y, Huang J, Tao Y, Yan W, Lu L et al (2016) Mutation in actin gamma-2 responsible for megacystis microcolon intestinal hypoperistalsis syndrome in 4 chinese patients. J Pediatr Gastroenterol Nutr 63:624–626CrossRefPubMed
52.
Zurück zum Zitat Matera I, Rusmini M, Guo Y, Lerone M, Li J, Zhang J et al (2016) Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstruction. Eur J Hum Genet 24:1211–1215CrossRefPubMedPubMedCentral Matera I, Rusmini M, Guo Y, Lerone M, Li J, Zhang J et al (2016) Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstruction. Eur J Hum Genet 24:1211–1215CrossRefPubMedPubMedCentral
53.
Zurück zum Zitat De Sousa J, Upadhyay V, Stone P (2016) Megacystis microcolon intestinal hypoperistalsis syndrome: case reports and discussion of the literature. Fetal Diagn Ther 39:152–157CrossRefPubMed De Sousa J, Upadhyay V, Stone P (2016) Megacystis microcolon intestinal hypoperistalsis syndrome: case reports and discussion of the literature. Fetal Diagn Ther 39:152–157CrossRefPubMed
54.
Zurück zum Zitat Tarlan S, Mahyar A, Chegini V, Chegini V (2015) megacystis microcolon intestinal hypoperistalsis syndrome: report of a rare case in newborn. Acta Med Iran 53:518–522PubMed Tarlan S, Mahyar A, Chegini V, Chegini V (2015) megacystis microcolon intestinal hypoperistalsis syndrome: report of a rare case in newborn. Acta Med Iran 53:518–522PubMed
55.
Zurück zum Zitat Soh H, Fukuzawa M, Kubota A, Kawahara H, Ueno T, Taguchi T (2015) Megacystis microcolon intestinal hypoperistalsis syndrome: a report of a nationwide survey in Japan. J Pediatr Surg 50:2048–2050CrossRefPubMed Soh H, Fukuzawa M, Kubota A, Kawahara H, Ueno T, Taguchi T (2015) Megacystis microcolon intestinal hypoperistalsis syndrome: a report of a nationwide survey in Japan. J Pediatr Surg 50:2048–2050CrossRefPubMed
56.
Zurück zum Zitat Taguchi T, Ieiri S, Miyoshi K, Kohashi K, Oda Y, Kubota A et al (2017) The incidence and outcome of allied disorders of hirschsprung’s disease in Japan: results from a nationwide survey. Asian J Surg 40:29–34CrossRefPubMed Taguchi T, Ieiri S, Miyoshi K, Kohashi K, Oda Y, Kubota A et al (2017) The incidence and outcome of allied disorders of hirschsprung’s disease in Japan: results from a nationwide survey. Asian J Surg 40:29–34CrossRefPubMed
57.
Zurück zum Zitat Liaqat N, Nayyar S, Iqbal A, Hameed Dar S (2015) Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): a rarity. J Neonatal Surg 4:11PubMedPubMedCentral Liaqat N, Nayyar S, Iqbal A, Hameed Dar S (2015) Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): a rarity. J Neonatal Surg 4:11PubMedPubMedCentral
58.
Zurück zum Zitat Tuzovic L, Tang S, Miller RS, Rohena L, Shahmirzadi L, Gonzalez K et al (2015) new insights into the genetics of fetal megacystis: ACTG2 mutations, encoding gamma-2 smooth muscle actin in megacystis microcolon intestinal hypoperistalsis syndrome (berdon syndrome). Fetal Diagn Ther 38:296–306CrossRefPubMed Tuzovic L, Tang S, Miller RS, Rohena L, Shahmirzadi L, Gonzalez K et al (2015) new insights into the genetics of fetal megacystis: ACTG2 mutations, encoding gamma-2 smooth muscle actin in megacystis microcolon intestinal hypoperistalsis syndrome (berdon syndrome). Fetal Diagn Ther 38:296–306CrossRefPubMed
59.
Zurück zum Zitat Lee S, Park HJ, Yoon J, Hong SH, Oh CY, Lee SK et al (2016) Reversal of intestinal failure-associated liver disease by switching from a combination lipid emulsion containing fish oil to fish oil monotherapy. JPEN J Parenter Enteral Nutr 40:437–440CrossRefPubMed Lee S, Park HJ, Yoon J, Hong SH, Oh CY, Lee SK et al (2016) Reversal of intestinal failure-associated liver disease by switching from a combination lipid emulsion containing fish oil to fish oil monotherapy. JPEN J Parenter Enteral Nutr 40:437–440CrossRefPubMed
60.
Zurück zum Zitat Gauthier J, Ouled Amar Bencheikh B, Hamdan FF, Harrison SM, Baker LA, Couture F et al (2015) A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome. Eur J Hum Genet 23:1266–1268CrossRefPubMed Gauthier J, Ouled Amar Bencheikh B, Hamdan FF, Harrison SM, Baker LA, Couture F et al (2015) A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome. Eur J Hum Genet 23:1266–1268CrossRefPubMed
61.
Zurück zum Zitat Wangler MF, Gonzaga-Jauregui C, Gambin T, Penney S, Moss T, Chopra A et al (2014) Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome. PLoS genetics 10:e1004258CrossRefPubMedPubMedCentral Wangler MF, Gonzaga-Jauregui C, Gambin T, Penney S, Moss T, Chopra A et al (2014) Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome. PLoS genetics 10:e1004258CrossRefPubMedPubMedCentral
62.
Zurück zum Zitat Thorson W, Diaz-Horta O, Foster J II, Spiliopoulos M, Quintero R, Farooq A et al (2014) De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis. Hum Genet 133:737–742CrossRefPubMed Thorson W, Diaz-Horta O, Foster J II, Spiliopoulos M, Quintero R, Farooq A et al (2014) De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis. Hum Genet 133:737–742CrossRefPubMed
63.
Zurück zum Zitat Ueno T, Wada M, Hoshino K, Sakamoto S, Furukawa H, Fukuzawa M (2013) A national survey of patients with intestinal motility disorders who are potential candidates for intestinal transplantation in Japan. Transplant Proc 45:2029–2031CrossRefPubMed Ueno T, Wada M, Hoshino K, Sakamoto S, Furukawa H, Fukuzawa M (2013) A national survey of patients with intestinal motility disorders who are potential candidates for intestinal transplantation in Japan. Transplant Proc 45:2029–2031CrossRefPubMed
64.
Zurück zum Zitat Hiradfar M, Shojaeian R, Dehghanian P, Hajian S (2013) Megacystis microcolon intestinal hypoperistalsis syndrome. BMJ Case Rep 2013 Hiradfar M, Shojaeian R, Dehghanian P, Hajian S (2013) Megacystis microcolon intestinal hypoperistalsis syndrome. BMJ Case Rep 2013
65.
Zurück zum Zitat McClelland C, Walsh RD, Chikwava KR, Johnson MP, Mattei P, Liu GT (2013) Congenital mydriasis associated with megacystis microcolon intestinal hypoperistalsis syndrome. J Neuroophthalmol 33:271–275CrossRefPubMed McClelland C, Walsh RD, Chikwava KR, Johnson MP, Mattei P, Liu GT (2013) Congenital mydriasis associated with megacystis microcolon intestinal hypoperistalsis syndrome. J Neuroophthalmol 33:271–275CrossRefPubMed
66.
Zurück zum Zitat Adeb M, Anupindi S, Carr M, Darge K (2012) An unusual urinary tract presentation in a case of megacystis microcolon intestinal hypoperistalsis syndrome. J Radiol Case Rep 6:1–7PubMedPubMedCentral Adeb M, Anupindi S, Carr M, Darge K (2012) An unusual urinary tract presentation in a case of megacystis microcolon intestinal hypoperistalsis syndrome. J Radiol Case Rep 6:1–7PubMedPubMedCentral
67.
Zurück zum Zitat Machado L, Matias A, Rodrigues M, Mariz C, Monteiro J, Montenegro N (2013) Fetal megacystis as a prenatal challenge: megacystis-microcolon-intestinal hypoperistalsis syndrome in a male fetus. Ultrasound Obstet Gynecol 41:345–347CrossRefPubMed Machado L, Matias A, Rodrigues M, Mariz C, Monteiro J, Montenegro N (2013) Fetal megacystis as a prenatal challenge: megacystis-microcolon-intestinal hypoperistalsis syndrome in a male fetus. Ultrasound Obstet Gynecol 41:345–347CrossRefPubMed
68.
Zurück zum Zitat Huang CM, Tseng SH, Weng CC, Chen Y (2013) Isolated intestinal transplantation for megacystis microcolon intestinal hypoperistalsis syndrome: case report. Pediatr Transpl 17:E4–E8CrossRef Huang CM, Tseng SH, Weng CC, Chen Y (2013) Isolated intestinal transplantation for megacystis microcolon intestinal hypoperistalsis syndrome: case report. Pediatr Transpl 17:E4–E8CrossRef
69.
Zurück zum Zitat Ballisty MM, Braithwaite KA, Shehata BM, Dickson PN (2013) Imaging findings in megacystis-microcolon-intestinal hypoperistalsis syndrome. Pediatr Radiol 43:454–459CrossRefPubMed Ballisty MM, Braithwaite KA, Shehata BM, Dickson PN (2013) Imaging findings in megacystis-microcolon-intestinal hypoperistalsis syndrome. Pediatr Radiol 43:454–459CrossRefPubMed
70.
Zurück zum Zitat Lopez-Munoz E, Hernandez-Zarco A, Polanco-Ortiz A, Villa-Morales J, Mateos-Sanchez L (2013) Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS): report of a case with prolonged survival and literature review. J Pediatr Urol 9:e12–e18CrossRefPubMed Lopez-Munoz E, Hernandez-Zarco A, Polanco-Ortiz A, Villa-Morales J, Mateos-Sanchez L (2013) Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS): report of a case with prolonged survival and literature review. J Pediatr Urol 9:e12–e18CrossRefPubMed
71.
Zurück zum Zitat Ravindra KV, Martin AE, Vikraman DS, Brennan TV, Collins BH, Rege AS et al (2012) Use of vascularized posterior rectus sheath allograft in pediatric multivisceral transplantation—report of two cases. Am J Transpl 12:2242–2246CrossRef Ravindra KV, Martin AE, Vikraman DS, Brennan TV, Collins BH, Rege AS et al (2012) Use of vascularized posterior rectus sheath allograft in pediatric multivisceral transplantation—report of two cases. Am J Transpl 12:2242–2246CrossRef
72.
Zurück zum Zitat Akhtar T, Alladi A, Siddappa OS (2012) Megacystis-microcolon-intestinal hypoperistalsis syndrome associated with prune belly syndrome: a case report. J Neonatal Surg 1:26PubMedPubMedCentral Akhtar T, Alladi A, Siddappa OS (2012) Megacystis-microcolon-intestinal hypoperistalsis syndrome associated with prune belly syndrome: a case report. J Neonatal Surg 1:26PubMedPubMedCentral
73.
Zurück zum Zitat Mantan M, Singhal KK, Sethi GR, Aggarwal SK (2011) Megacystis, microcolon, intestinal hypoperistalsis syndrome and bilateral streak gonads. Indian J Nephrol 21:212–214CrossRefPubMedPubMedCentral Mantan M, Singhal KK, Sethi GR, Aggarwal SK (2011) Megacystis, microcolon, intestinal hypoperistalsis syndrome and bilateral streak gonads. Indian J Nephrol 21:212–214CrossRefPubMedPubMedCentral
74.
Zurück zum Zitat Jain VK, Garge S, Singh S, Lahoti B (2011) Megacystis microcolon intestinal hypoperistalsis syndrome complicated by perforation. Afr J Paediatr Surg 8:70–71CrossRefPubMed Jain VK, Garge S, Singh S, Lahoti B (2011) Megacystis microcolon intestinal hypoperistalsis syndrome complicated by perforation. Afr J Paediatr Surg 8:70–71CrossRefPubMed
75.
Zurück zum Zitat Maruyama H, Hasegawa Y, Sugibayashi R, Iwasaki Y, Fujino S, Amari S et al (2018) Megacystis microcolon intestinal hypoperistalsis syndrome overlapping prune belly syndrome. J Pediatr Surg Case Rep 34:54–57CrossRef Maruyama H, Hasegawa Y, Sugibayashi R, Iwasaki Y, Fujino S, Amari S et al (2018) Megacystis microcolon intestinal hypoperistalsis syndrome overlapping prune belly syndrome. J Pediatr Surg Case Rep 34:54–57CrossRef
76.
Zurück zum Zitat Yetman AT, Starr LJ (2018) Newly described recessive MYH11 disorder with clinical overlap of multisystemic smooth muscle dysfunction and megacystis microcolon hypoperistalsis syndromes. Am J Med Genet A 176:1011–1014CrossRefPubMed Yetman AT, Starr LJ (2018) Newly described recessive MYH11 disorder with clinical overlap of multisystemic smooth muscle dysfunction and megacystis microcolon hypoperistalsis syndromes. Am J Med Genet A 176:1011–1014CrossRefPubMed
77.
Zurück zum Zitat Farrelly JS, Weiss RM, Copel JA, Porto AF, Ahle SL, Luks VL et al (2018) An atypical case of megacystis microcolon intestinal hypoperistalsis syndrome with extended survival and consistent bowel function. J Pediatr Surg Case Rep 30:48–51CrossRef Farrelly JS, Weiss RM, Copel JA, Porto AF, Ahle SL, Luks VL et al (2018) An atypical case of megacystis microcolon intestinal hypoperistalsis syndrome with extended survival and consistent bowel function. J Pediatr Surg Case Rep 30:48–51CrossRef
78.
Zurück zum Zitat Takasaki C, Yoshihara T, Yawaka Y (2018) Oral findings in a patient with megacystis microcolon intestinal hypoperistalsis syndrome: a case report. Pediatr Dental J 28:57–61CrossRef Takasaki C, Yoshihara T, Yawaka Y (2018) Oral findings in a patient with megacystis microcolon intestinal hypoperistalsis syndrome: a case report. Pediatr Dental J 28:57–61CrossRef
79.
Zurück zum Zitat Plachno K, Spodaryk M, Pabisek-Miernik J, Laskowska J, Wolnicki M (2017) Coexistence of berdon syndrome and prune belly syndrome null case studies zespol berdona oraz zespol suszonej sliwki i ich wspolistnienie null analiza przypadkow. Pediatr Pol 92:764–769CrossRef Plachno K, Spodaryk M, Pabisek-Miernik J, Laskowska J, Wolnicki M (2017) Coexistence of berdon syndrome and prune belly syndrome null case studies zespol berdona oraz zespol suszonej sliwki i ich wspolistnienie null analiza przypadkow. Pediatr Pol 92:764–769CrossRef
80.
Zurück zum Zitat Simsek C, Yavuz A, Korgali E, Guney C, Atalar M (2017) Berdon syndrome: megacystis-microcolonintestinal hypoperistalsis; case report. Erciyes Med J 39:S19 (Abstract) Simsek C, Yavuz A, Korgali E, Guney C, Atalar M (2017) Berdon syndrome: megacystis-microcolonintestinal hypoperistalsis; case report. Erciyes Med J 39:S19 (Abstract)
81.
Zurück zum Zitat Cisneros ML, Figueroa A, Cruzado JP, Pajuelo R, Matos A, Lipa R (2016) Syndrome megacystis-microcolon-hypoperistalsis: case report. Pediatr Nephrol 31:1791–1792 Cisneros ML, Figueroa A, Cruzado JP, Pajuelo R, Matos A, Lipa R (2016) Syndrome megacystis-microcolon-hypoperistalsis: case report. Pediatr Nephrol 31:1791–1792
82.
Zurück zum Zitat Andreoiu OM, Vasile CG, Vasile A, Enculescu A, Becheanu G, Ionescu S (2016) Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): case report. Virchows Arch 469:S322 Andreoiu OM, Vasile CG, Vasile A, Enculescu A, Becheanu G, Ionescu S (2016) Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): case report. Virchows Arch 469:S322
83.
Zurück zum Zitat Warner S, Lawson S, Ogboli M, Alfred A, Taylor P, Harltley J et al (2016) Skin GVHD in paediatric intestinal transplant recipients-experience from a national UK centre. Transplantation 100:S256CrossRef Warner S, Lawson S, Ogboli M, Alfred A, Taylor P, Harltley J et al (2016) Skin GVHD in paediatric intestinal transplant recipients-experience from a national UK centre. Transplantation 100:S256CrossRef
84.
Zurück zum Zitat Garcia Delgado R, Garcia Rodriguez R, GArmas Roca M, Romero Requejo A, Garcia Escribano P, Santana Suarez A et al (2015) Megacystis-micro colon-intestinal hypoperistalsis syndrome: a case report. J Perinatal Med 43(Suppl. 1) Garcia Delgado R, Garcia Rodriguez R, GArmas Roca M, Romero Requejo A, Garcia Escribano P, Santana Suarez A et al (2015) Megacystis-micro colon-intestinal hypoperistalsis syndrome: a case report. J Perinatal Med 43(Suppl. 1)
85.
Zurück zum Zitat Kocoshis SA, Goldschmidt ML, Nathan JD, Tiao GM, Alonso MH, Kaul A (2015) Esophageal dysmotility following intestinal transplantation for the megacystis microcolon hypoperistalsis syndrome (MMIHS): an expanded clinical spectrum. Transplantation 99:S113 Kocoshis SA, Goldschmidt ML, Nathan JD, Tiao GM, Alonso MH, Kaul A (2015) Esophageal dysmotility following intestinal transplantation for the megacystis microcolon hypoperistalsis syndrome (MMIHS): an expanded clinical spectrum. Transplantation 99:S113
86.
Zurück zum Zitat Joody M, Moradi M, Kazemzadeh B (2014) Megacystis microcolon intestinal hypoperistalsis syndrome may underdiagnosed. Int J Urol 21:A245 Joody M, Moradi M, Kazemzadeh B (2014) Megacystis microcolon intestinal hypoperistalsis syndrome may underdiagnosed. Int J Urol 21:A245
87.
Zurück zum Zitat Stewart MS, Dietz RM, Landman MP, Moulton SL, Wright CJ (2014) Abdominal radiograph with intravesical air and possible small bowel atresia. J Pediatr 164:1238–1238. e1CrossRefPubMedPubMedCentral Stewart MS, Dietz RM, Landman MP, Moulton SL, Wright CJ (2014) Abdominal radiograph with intravesical air and possible small bowel atresia. J Pediatr 164:1238–1238. e1CrossRefPubMedPubMedCentral
88.
Zurück zum Zitat Morali-Karzei N, Kummer S, Hadzik B, Bizjak G, Hoehn T (2013) Prenatal ultrasonographic diagnosis of megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS). Z Geburtshilfe Neonatol 217:1CrossRef Morali-Karzei N, Kummer S, Hadzik B, Bizjak G, Hoehn T (2013) Prenatal ultrasonographic diagnosis of megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS). Z Geburtshilfe Neonatol 217:1CrossRef
89.
Zurück zum Zitat Iskander P, Ghahremani S, Boechat I (2013) Megacystis microcolon intestinal hypoperistalsis syndrome. Pediatr Radiol 43:S369–S370 Iskander P, Ghahremani S, Boechat I (2013) Megacystis microcolon intestinal hypoperistalsis syndrome. Pediatr Radiol 43:S369–S370
90.
Zurück zum Zitat Birkemeier K (2013) Achalasia in megacystis microcolon intestinal hypoperistalsis syndrome: a case report. Pediatr Radiol 43:S372 Birkemeier K (2013) Achalasia in megacystis microcolon intestinal hypoperistalsis syndrome: a case report. Pediatr Radiol 43:S372
91.
Zurück zum Zitat Lozoya Araque T, Vila-Vives JM, Perales-Puchalt A, Soler Ferrero I, Quiroga R, Llorens-Salvador R et al (2013) Berdon syndrome: Intrauterine diagnosis and postnatal outcome sindrome de berdon: diagnostico intrauterino y evolucion posnatal. Diagnostico Prenatal 24:23–28CrossRef Lozoya Araque T, Vila-Vives JM, Perales-Puchalt A, Soler Ferrero I, Quiroga R, Llorens-Salvador R et al (2013) Berdon syndrome: Intrauterine diagnosis and postnatal outcome sindrome de berdon: diagnostico intrauterino y evolucion posnatal. Diagnostico Prenatal 24:23–28CrossRef
92.
Zurück zum Zitat Jarmoloinski T, Zaniew M, Paradowski S, Balachowska-Kosciolek I (2012) Berdon syndrome: from intrauterine ultrasonography to clinical diagnosis. Przeglad Pediatryczny 42:103–106 Jarmoloinski T, Zaniew M, Paradowski S, Balachowska-Kosciolek I (2012) Berdon syndrome: from intrauterine ultrasonography to clinical diagnosis. Przeglad Pediatryczny 42:103–106
93.
Zurück zum Zitat Kitazono M, Bellah R (2012) Prenatal and postnatal imaging findings in megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS). Pediatr Radiol 42:S333 Kitazono M, Bellah R (2012) Prenatal and postnatal imaging findings in megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS). Pediatr Radiol 42:S333
94.
Zurück zum Zitat Braithwaite K, Dickson P, Ballisty MM (2012) Imaging findings in megacystic microcolon intestinal hypoperistalsis syndrome, a rare disease. Pediatr Radiol 42:S333–S334 Braithwaite K, Dickson P, Ballisty MM (2012) Imaging findings in megacystic microcolon intestinal hypoperistalsis syndrome, a rare disease. Pediatr Radiol 42:S333–S334
Metadaten
Titel
Consanguinity and its relevance for the incidence of megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS): systematic review
verfasst von
Hiroki Nakamura
Anne Marie O’Donnell
Prem Puri
Publikationsdatum
01.11.2018
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Surgery International / Ausgabe 2/2019
Print ISSN: 0179-0358
Elektronische ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-018-4390-6

Weitere Artikel der Ausgabe 2/2019

Pediatric Surgery International 2/2019 Zur Ausgabe

ADHS-Medikation erhöht das kardiovaskuläre Risiko

16.05.2024 Herzinsuffizienz Nachrichten

Erwachsene, die Medikamente gegen das Aufmerksamkeitsdefizit-Hyperaktivitätssyndrom einnehmen, laufen offenbar erhöhte Gefahr, an Herzschwäche zu erkranken oder einen Schlaganfall zu erleiden. Es scheint eine Dosis-Wirkungs-Beziehung zu bestehen.

Erstmanifestation eines Diabetes-Typ-1 bei Kindern: Ein Notfall!

16.05.2024 DDG-Jahrestagung 2024 Kongressbericht

Manifestiert sich ein Typ-1-Diabetes bei Kindern, ist das ein Notfall – ebenso wie eine diabetische Ketoazidose. Die Grundsäulen der Therapie bestehen aus Rehydratation, Insulin und Kaliumgabe. Insulin ist das Medikament der Wahl zur Behandlung der Ketoazidose.

Frühe Hypertonie erhöht späteres kardiovaskuläres Risiko

Wie wichtig es ist, pädiatrische Patienten auf Bluthochdruck zu screenen, zeigt eine kanadische Studie: Hypertone Druckwerte in Kindheit und Jugend steigern das Risiko für spätere kardiovaskuläre Komplikationen.

Betalaktam-Allergie: praxisnahes Vorgehen beim Delabeling

16.05.2024 Pädiatrische Allergologie Nachrichten

Die große Mehrheit der vermeintlichen Penicillinallergien sind keine. Da das „Etikett“ Betalaktam-Allergie oft schon in der Kindheit erworben wird, kann ein frühzeitiges Delabeling lebenslange Vorteile bringen. Ein Team von Pädiaterinnen und Pädiatern aus Kanada stellt vor, wie sie dabei vorgehen.

Update Pädiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.