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Erschienen in: European Journal of Pediatrics 12/2003

01.12.2003 | Original Paper

Malignant hypertension and cerebral haemorrhage in Seckel syndrome

verfasst von: Rossella Di Bartolomeo, Giancarlo Polidori, Marco Piastra, Luigi Viola, Guiseppe Zampino, Antonio Chiaretti

Erschienen in: European Journal of Pediatrics | Ausgabe 12/2003

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Abstract

Seckel syndrome is an autosomal recessive condition with severe short stature and facial and neurological anomalies. Intracranial haemorrhage, due to rupture of a cerebral aneurysm, is a very rare complication of this syndrome. Malignant hypertension may play an important role in the aetiology of the aneurysm and early detection is essential in order to prevent organ damage. Conclusion:we report a new case of Seckel syndrome associated with malignant hypertension and cerebral haemorrhage.
Literatur
1.
Zurück zum Zitat Borglum AD, Balslev T, Haagerup A, Birkebaek N, Binderup H, Kruse TA, Hertz JM (2001) A new locus for Seckel syndrome on chromosome 18p 11.31-q11.2. Eur J Hum Gen 9: 753–757CrossRef Borglum AD, Balslev T, Haagerup A, Birkebaek N, Binderup H, Kruse TA, Hertz JM (2001) A new locus for Seckel syndrome on chromosome 18p 11.31-q11.2. Eur J Hum Gen 9: 753–757CrossRef
2.
Zurück zum Zitat D’Angelo V, Ceddia AMP, Zelante L, Florio FP (1998) Multiple intracranial aneurysms in a patient with Seckel syndrome. Childs Nerv Syst 14: 82–84CrossRefPubMed D’Angelo V, Ceddia AMP, Zelante L, Florio FP (1998) Multiple intracranial aneurysms in a patient with Seckel syndrome. Childs Nerv Syst 14: 82–84CrossRefPubMed
3.
Zurück zum Zitat Faivre L, Le Merrer M, Lyonnet S, Plauchu H, Dagonneau N, Campos-Xavier AB, Attia-Sobol J, Verloes A, Munnich A, Cormier Daire V (2002) Clinical and genetic heterogeneity of Seckel syndrome. Am J Med Genet 112: 379–383CrossRefPubMed Faivre L, Le Merrer M, Lyonnet S, Plauchu H, Dagonneau N, Campos-Xavier AB, Attia-Sobol J, Verloes A, Munnich A, Cormier Daire V (2002) Clinical and genetic heterogeneity of Seckel syndrome. Am J Med Genet 112: 379–383CrossRefPubMed
4.
Zurück zum Zitat Goodship J, Gill H, Carter J, Jackson A, Splitt M, Wright M (2000) Autozygosity mapping of a Seckel syndrome locus to chromosome 3q22.1-q24. Am J Hum Genet 67: 498–503CrossRefPubMed Goodship J, Gill H, Carter J, Jackson A, Splitt M, Wright M (2000) Autozygosity mapping of a Seckel syndrome locus to chromosome 3q22.1-q24. Am J Hum Genet 67: 498–503CrossRefPubMed
5.
Zurück zum Zitat National High Blood Pressure Education Program Working Group on Hypertension Control in Children and Adolescents (1996) Update on the 1987 task force report on high pressure in children and adolescents: a working group from the national high blood pressure education program. Pediatrics 98: 649–658PubMed National High Blood Pressure Education Program Working Group on Hypertension Control in Children and Adolescents (1996) Update on the 1987 task force report on high pressure in children and adolescents: a working group from the national high blood pressure education program. Pediatrics 98: 649–658PubMed
6.
Zurück zum Zitat Sorof JM, Dow-Smith C, Moore PJ (1999) Severe hypertensive sequelae in a child with Seckel syndrome (bird-like dwarfism). Pediatr Nephrol 13: 343–346CrossRefPubMed Sorof JM, Dow-Smith C, Moore PJ (1999) Severe hypertensive sequelae in a child with Seckel syndrome (bird-like dwarfism). Pediatr Nephrol 13: 343–346CrossRefPubMed
Metadaten
Titel
Malignant hypertension and cerebral haemorrhage in Seckel syndrome
verfasst von
Rossella Di Bartolomeo
Giancarlo Polidori
Marco Piastra
Luigi Viola
Guiseppe Zampino
Antonio Chiaretti
Publikationsdatum
01.12.2003
Verlag
Springer-Verlag
Erschienen in
European Journal of Pediatrics / Ausgabe 12/2003
Print ISSN: 0340-6199
Elektronische ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-003-1310-z

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