Literature DB >> 11787035

Split-hand/split-foot malformation with paternal mutation in the p63 gene.

I Witters1, H Van Bokhoven, A Goossens, F A Van Assche, J P Fryns.   

Abstract

We report the prenatal diagnosis at 16 weeks' gestation of bilateral split-hand/split-foot malformation (SHSFM) with severe lobster claw deformity of hands and feet in a male fetus without associated malformations. A minor manifestation of SHSFM was present in the father with only mild bilateral foot involvement (syndactyly I-II; cleft II-III; left cutaneous syndactyly III-IV). Mutation analysis of the p63 gene on chromosome 3q27 showed a missense mutation 577A-->G (predicting amino acid substitution K193E) in the father. This mutation has not been reported so far in SHSFM but resembles the previously reported 580A-->G (predicting amino acid substitution K194E) in a family with SHSFM. Copyright 2001 John Wiley & Sons, Ltd.

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Year:  2001        PMID: 11787035     DOI: 10.1002/pd.181

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  3 in total

1.  p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.

Authors:  H van Bokhoven; B C Hamel; M Bamshad; E Sangiorgi; F Gurrieri; P H Duijf; K R Vanmolkot; E van Beusekom; S E van Beersum; J Celli; G F Merkx; R Tenconi; J P Fryns; A Verloes; R A Newbury-Ecob; A Raas-Rotschild; F Majewski; F A Beemer; A Janecke; D Chitayat; G Crisponi; H Kayserili; J R Yates; G Neri; H G Brunner
Journal:  Am J Hum Genet       Date:  2001-07-17       Impact factor: 11.025

2.  DLX5, FGF8 and the Pin1 isomerase control ΔNp63α protein stability during limb development: a regulatory loop at the basis of the SHFM and EEC congenital malformations.

Authors:  Michela Restelli; Teresa Lopardo; Nadia Lo Iacono; Giulia Garaffo; Daniele Conte; Alessandra Rustighi; Marco Napoli; Giannino Del Sal; David Perez-Morga; Antonio Costanzo; Giorgio Roberto Merlo; Luisa Guerrini
Journal:  Hum Mol Genet       Date:  2014-02-25       Impact factor: 6.150

3.  Analysis of large phenotypic variability of EEC and SHFM4 syndromes caused by K193E mutation of the TP63 gene.

Authors:  Jianhua Wei; Yang Xue; Lian Wu; Jie Ma; Xiuli Yi; Junrui Zhang; Bin Lu; Chunying Li; Dashuang Shi; Songtao Shi; Xinghua Feng; Tao Cai
Journal:  PLoS One       Date:  2012-05-04       Impact factor: 3.240

  3 in total

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