Literature DB >> 6263040

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

P Merlob, M Grünebaum, S H Reisner.   

Abstract

A newborn infant with craniofacial dysmorphism and polysndactyly (Greig's Syndrome) is reported. This syndrome is manifested by postaxial polydactyly of the fingers and preaxial polydactyly of the toes, with syndactyly. The craniofacial dysmorphism is characterized by frontal bossing and other variable manifestations. X-ray examination revealed markedly advanced bone age. The mode of inheritance appears to be autosomal dominant.

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Year:  1981        PMID: 6263040     DOI: 10.1111/j.1651-2227.1981.tb05557.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  2 in total

1.  Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.

Authors:  U Radhakrishna; J L Blouin; H Mehenni; U C Patel; M N Patel; J V Solanki; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

2.  Familial crossed polysyndactyly in four generations of an Indian family.

Authors:  Pooja Dewan; Nitin Agarwal; Preeti Dewan; Vineet Batta
Journal:  World J Pediatr       Date:  2010-02-01       Impact factor: 2.764

  2 in total

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