Skip to main content
Erschienen in: Journal of Children's Orthopaedics 5/2008

01.10.2008 | Current Concept Review

Epidemiology, etiology, and genetic aspects of reduction deficiencies of the lower limb

verfasst von: Ismat Ghanem

Erschienen in: Journal of Children's Orthopaedics | Ausgabe 5/2008

Einloggen, um Zugang zu erhalten

Abstract

Although the majority of lower limb deficiencies are of sporadic occurrence and of unknown etiology, genetic factors are involved in a significant number, with variable modes of inheritance. A better-informed public is demanding advice concerning cause and recurrence. Careful scrutiny of the medical history and family tree and attention to phenotypic details may help to delineate entities. At times, specific chromosomal tests are important, mainly when there is bilateral or multiorgan involvement or when limb deficiency is associated with developmental delay and/or mental retardation. This paper is intended to refamiliarize the orthopaedic community with basic genetic aspects regulating reduction deficiencies of the lower limbs, and to emphasize on the importance and indications of genetic counseling.
Literatur
1.
Zurück zum Zitat Brent RL (1985) Prevention of physical and mental congenital defects. Part A/ The scope of the problem. In Marois M (ed) Progress in clinical and biological research. Alan R. Liss., New York, 163A:55–68 Brent RL (1985) Prevention of physical and mental congenital defects. Part A/ The scope of the problem. In Marois M (ed) Progress in clinical and biological research. Alan R. Liss., New York, 163A:55–68
2.
Zurück zum Zitat Clavert JM. (2000) Embryologie normale et pathologique des membres inférieurs. Essai de classification des malformations. In: Duparc J (ed) Cahiers d’enseignement de la SOFCOT. Carlioz H and Clavert JM. Malformations congénitales des membres inférieurs. Elsevier, Paris, 74:3–15 Clavert JM. (2000) Embryologie normale et pathologique des membres inférieurs. Essai de classification des malformations. In: Duparc J (ed) Cahiers d’enseignement de la SOFCOT. Carlioz H and Clavert JM. Malformations congénitales des membres inférieurs. Elsevier, Paris, 74:3–15
3.
Zurück zum Zitat Rogala EJ, Wynne-Davies R, Littlejohn A, Gormley J (1974) Congenital limb anomalies: frequency and etiological factors. Data from the Edinburgh Register of the Newborn (1964–1968). J Med Genet 11:221–233CrossRef Rogala EJ, Wynne-Davies R, Littlejohn A, Gormley J (1974) Congenital limb anomalies: frequency and etiological factors. Data from the Edinburgh Register of the Newborn (1964–1968). J Med Genet 11:221–233CrossRef
4.
Zurück zum Zitat Scott CI (1989) Genetic and familial aspects of limb defects with emphasis on the lower extremities. In: Kalamchi A (ed) Congenital lower limb deficiencies. Springer, New York, pp 46–57CrossRef Scott CI (1989) Genetic and familial aspects of limb defects with emphasis on the lower extremities. In: Kalamchi A (ed) Congenital lower limb deficiencies. Springer, New York, pp 46–57CrossRef
5.
Zurück zum Zitat Glessner JR (1963) Spontaneous intra-uterine amputation. J Bone Joint Surg Am 45:351–353 Glessner JR (1963) Spontaneous intra-uterine amputation. J Bone Joint Surg Am 45:351–353
6.
Zurück zum Zitat Weaver DD (1998) Vascular etiology of limb defects: the subclavian artery supply disruption sequence. In: Herring JA, Birch JG (eds) The child with a limb deficiency. A AOS, Rosemont, pp 25–32 Weaver DD (1998) Vascular etiology of limb defects: the subclavian artery supply disruption sequence. In: Herring JA, Birch JG (eds) The child with a limb deficiency. A AOS, Rosemont, pp 25–32
7.
Zurück zum Zitat Otsuji M, Takahara M, Naruse T, Guan D, Harada M, Zhe P, Takagi M, Ogino T (2005) Developmental abnormalities in rat embryos leading to tibial ray deficiencies induced by busulfan. Birth Defects Res A Clin Mol Teratol 73:461–467CrossRef Otsuji M, Takahara M, Naruse T, Guan D, Harada M, Zhe P, Takagi M, Ogino T (2005) Developmental abnormalities in rat embryos leading to tibial ray deficiencies induced by busulfan. Birth Defects Res A Clin Mol Teratol 73:461–467CrossRef
8.
Zurück zum Zitat Hoffmann K, Müller JS, Stricker S, Megarbane A, Rajab A, Lindner TH, Cohen M, Chouery E, Adaimy L, Ghanem I, Delague V, Boltshauser E, Talim B, Horvath R, Robinson PN, Lochmu¨ller H, Hübner C, Mundlos S (2006) Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal g subunit. Am J Hum Genet 79:303–312CrossRef Hoffmann K, Müller JS, Stricker S, Megarbane A, Rajab A, Lindner TH, Cohen M, Chouery E, Adaimy L, Ghanem I, Delague V, Boltshauser E, Talim B, Horvath R, Robinson PN, Lochmu¨ller H, Hübner C, Mundlos S (2006) Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal g subunit. Am J Hum Genet 79:303–312CrossRef
9.
Zurück zum Zitat Biesecker LG (2002) Polydactyly: how many disorders and how many genes? Am J Med Genet 112:279–283CrossRef Biesecker LG (2002) Polydactyly: how many disorders and how many genes? Am J Med Genet 112:279–283CrossRef
10.
Zurück zum Zitat Megarbane A, Ghanem I (2004) A newly recognized chondrodysplasia with multiple dislocations. Am J Med Genet 130:107–109CrossRef Megarbane A, Ghanem I (2004) A newly recognized chondrodysplasia with multiple dislocations. Am J Med Genet 130:107–109CrossRef
11.
Zurück zum Zitat Megarbane A, Ghanem I, Rizk T, Jabbour P (2002) Prenatal growth deficiency with narrowness of the cervical spine, subglottic stenosis, hip dislocation, and severe delayed bone ossification: a new skeletal dysplasia. Am J Med Genet 112:70–74CrossRef Megarbane A, Ghanem I, Rizk T, Jabbour P (2002) Prenatal growth deficiency with narrowness of the cervical spine, subglottic stenosis, hip dislocation, and severe delayed bone ossification: a new skeletal dysplasia. Am J Med Genet 112:70–74CrossRef
12.
Zurück zum Zitat Hoon A, Hall JG (1988) Familial limb deficiency. Clin Genet 34:141–142CrossRef Hoon A, Hall JG (1988) Familial limb deficiency. Clin Genet 34:141–142CrossRef
13.
Zurück zum Zitat Tackels-Horne D, Toburen A, Sangiorgi E, Gurrieri F, de Mollerat X, Fischetto R, Causio F, Clarkson K, Stevenson RE, Schwartz CE (2001) Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21. Clin Genet 59:28–36CrossRef Tackels-Horne D, Toburen A, Sangiorgi E, Gurrieri F, de Mollerat X, Fischetto R, Causio F, Clarkson K, Stevenson RE, Schwartz CE (2001) Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21. Clin Genet 59:28–36CrossRef
14.
Zurück zum Zitat Richieri-Costa A, de Miranda E, Kamiya TY, Freire-Maia DV (1990) Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family. Am J Med Genet 36:1–6CrossRef Richieri-Costa A, de Miranda E, Kamiya TY, Freire-Maia DV (1990) Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family. Am J Med Genet 36:1–6CrossRef
15.
Zurück zum Zitat Naveed M, Al-Ali MT, Murthy SK, Al-Hajali S, Al-Khaja N, Deutsch S, Bottani A, Antonarakis SE, Nath SK, Radhakrishna U (2006) Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis. Am J Med Genet 140:1440–1446CrossRef Naveed M, Al-Ali MT, Murthy SK, Al-Hajali S, Al-Khaja N, Deutsch S, Bottani A, Antonarakis SE, Nath SK, Radhakrishna U (2006) Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis. Am J Med Genet 140:1440–1446CrossRef
16.
Zurück zum Zitat Zenteno JC, Berdon-Zapata V, Kofman-Alfaro S, Mutchinick OM (2005) Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of TP63. Am J Med Genet 134:74–76CrossRef Zenteno JC, Berdon-Zapata V, Kofman-Alfaro S, Mutchinick OM (2005) Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of TP63. Am J Med Genet 134:74–76CrossRef
17.
Zurück zum Zitat Richieri-Costa A (1987) Tibial hemimelia-cleft lip/palate in a Brazilian child born to consanguineous parents. Am J Med Genet 28:325–329CrossRef Richieri-Costa A (1987) Tibial hemimelia-cleft lip/palate in a Brazilian child born to consanguineous parents. Am J Med Genet 28:325–329CrossRef
18.
Zurück zum Zitat Faiyaz-Ul-Haque M, Zaidi SH, King LM, Haque S, Patel M, Ahmad M, Siddique T, Ahmad W, Tsui LC, Cohn DH (2005) Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes. Clin Genet 67:93–97CrossRef Faiyaz-Ul-Haque M, Zaidi SH, King LM, Haque S, Patel M, Ahmad M, Siddique T, Ahmad W, Tsui LC, Cohn DH (2005) Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes. Clin Genet 67:93–97CrossRef
19.
Zurück zum Zitat Naveed M, Nath SK, Gaines M, Al-Ali MT, Al-Khaja N, Hutchings D, Golla J, Deutsch S, Bottani A, Antonarakis SE, Ratnamala U, Radhakrishna U (2007) Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1. Am J Hum Genet 80:105–111CrossRef Naveed M, Nath SK, Gaines M, Al-Ali MT, Al-Khaja N, Hutchings D, Golla J, Deutsch S, Bottani A, Antonarakis SE, Ratnamala U, Radhakrishna U (2007) Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1. Am J Hum Genet 80:105–111CrossRef
20.
Zurück zum Zitat Say B, Tuncbilik E, Pirnar T (1971) Hereditary congenital coxa vara with dominant inheritance? Hum Genet 11:266–268CrossRef Say B, Tuncbilik E, Pirnar T (1971) Hereditary congenital coxa vara with dominant inheritance? Hum Genet 11:266–268CrossRef
21.
Zurück zum Zitat Freire-Maia A (1981) The extraordinary handless and footless families of Brazil. 50 years of acheiropodia. Am J Med Genet 9:31–41CrossRef Freire-Maia A (1981) The extraordinary handless and footless families of Brazil. 50 years of acheiropodia. Am J Med Genet 9:31–41CrossRef
22.
Zurück zum Zitat Megarbane A., Ghanem I (2002) Tibial/femoral hypoplasia with “hook” pelvis: a potentially unique dysostosis. Am J Med Genet 112:394–396CrossRef Megarbane A., Ghanem I (2002) Tibial/femoral hypoplasia with “hook” pelvis: a potentially unique dysostosis. Am J Med Genet 112:394–396CrossRef
23.
Zurück zum Zitat Brewster TG, Lachman RS, Kushner DC, Holmes LB, Isler RJ, Rimoin DL (1985) Oto-palato-digital syndrome, type II–an X-linked skeletal dysplasia. Am J Med Genet 20:249–254CrossRef Brewster TG, Lachman RS, Kushner DC, Holmes LB, Isler RJ, Rimoin DL (1985) Oto-palato-digital syndrome, type II–an X-linked skeletal dysplasia. Am J Med Genet 20:249–254CrossRef
24.
Zurück zum Zitat Matsuyama J, Mabuchi A, Zhang J, Iida A, Ikeda T, Kimizuka M, Ikegawa S (2003) A pair of sibs with tibial hemimelia born to phenotypically normal parents. J Hum Genet 48:173–176CrossRef Matsuyama J, Mabuchi A, Zhang J, Iida A, Ikeda T, Kimizuka M, Ikegawa S (2003) A pair of sibs with tibial hemimelia born to phenotypically normal parents. J Hum Genet 48:173–176CrossRef
25.
Zurück zum Zitat Basel D, Kilpatrick MW, Tsipouras P (2006) The expanding panorama of split hand foot malformation. Am J Med Genet 140:1359–1365CrossRef Basel D, Kilpatrick MW, Tsipouras P (2006) The expanding panorama of split hand foot malformation. Am J Med Genet 140:1359–1365CrossRef
Metadaten
Titel
Epidemiology, etiology, and genetic aspects of reduction deficiencies of the lower limb
verfasst von
Ismat Ghanem
Publikationsdatum
01.10.2008
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Children's Orthopaedics / Ausgabe 5/2008
Print ISSN: 1863-2521
Elektronische ISSN: 1863-2548
DOI
https://doi.org/10.1007/s11832-008-0098-9

Weitere Artikel der Ausgabe 5/2008

Journal of Children's Orthopaedics 5/2008 Zur Ausgabe

Arthropedia

Grundlagenwissen der Arthroskopie und Gelenkchirurgie. Erweitert durch Fallbeispiele, Videos und Abbildungen. 
» Jetzt entdecken

Update Orthopädie und Unfallchirurgie

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