Literature DB >> 20127219

Familial crossed polysyndactyly in four generations of an Indian family.

Pooja Dewan1, Nitin Agarwal, Preeti Dewan, Vineet Batta.   

Abstract

BACKGROUND: Polydactyly is the most common malformation of the limbs. "Crossed" polydactyly of hands and feet, i.e., preaxial in one and postaxial in the other, is extremely rare. It has not been included in the standard classification of hand and feet anomalies.
METHODS: We report an Indian family with 7 affected members across 4 generations who had "crossed polysyndactyly". All but one affected member had involvement of all four limbs. There were no other congenital anomalies in any of the family members.
RESULTS: Familial crossed polysyndactyly appeared to follow an autosomal dominant transmission. This is probably the first case of familial crossed polysyndactyly without any associated anomalies.
CONCLUSION: Familial crossed polysyndactyly is a rare malformation and all family members should be screened for other congenital malformations.

Entities:  

Mesh:

Year:  2010        PMID: 20127219     DOI: 10.1007/s12519-010-0020-7

Source DB:  PubMed          Journal:  World J Pediatr            Impact factor:   2.764


  10 in total

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Authors:  P A Nathan; R C Keniston
Journal:  J Bone Joint Surg Am       Date:  1975-09       Impact factor: 5.284

2.  A FAMILY WITH POLYSYNDACTYLY AND OTHER ANOMALIES.

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Journal:  J Hered       Date:  1965 Jan-Feb       Impact factor: 2.645

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5.  Unique case of polydactyly and a new classification system.

Authors:  Lawrence L Haber; Heiko B Adams; George H Thompson; Lori S Duncan; Lawrence A Didomenico; William P McCluskey
Journal:  J Pediatr Orthop       Date:  2007 Apr-May       Impact factor: 2.324

6.  Crossed polydactyly type I in a mother and son: an autosomal dominant trait?

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Journal:  Am J Med Genet       Date:  1991-07-01

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Journal:  Teratology       Date:  1977-10

8.  Associated anomalies in individuals with polydactyly.

Authors:  E E Castilla; R Lugarinho; M da Graça Dutra; L J Salgado
Journal:  Am J Med Genet       Date:  1998-12-28

9.  Familial crossed polysyndactyly.

Authors:  D J Goldstein; M Kambouris; R E Ward
Journal:  Am J Med Genet       Date:  1994-04-15

10.  A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome).

Authors:  P Merlob; M Grünebaum; S H Reisner
Journal:  Acta Paediatr Scand       Date:  1981-03
  10 in total

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