Literature DB >> 3366140

Anomalous inheritance in a kindred with split hand, split foot malformation.

M Spranger1, J Schapera.   

Abstract

A South African family with autosomal dominant split hand, split foot (SHSF) malformation has been studied. The pedigree was unusual in that three unaffected siblings with normal parents had each produced affected offspring. New mutation, germinal mosaicism and autosomal recessive inheritance are unlikely. Possible explanations of this contentious situation may be an unstable premutation or non-penetrance due to an inhibiting factor associated with the gene responsible for SHSF. Pregnancy monitoring by ultrasound of unaffected close relatives of a person with SHSF is recommended.

Entities:  

Mesh:

Year:  1988        PMID: 3366140     DOI: 10.1007/bf00442225

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  15 in total

1.  CLEFT HAND: CLASSIFICATION, INCIDENCE, AND TREATMENT. REVIEW OF THE LITERATURE AND REPORT OF NINETEEN CASES.

Authors:  A J BARSKY
Journal:  J Bone Joint Surg Am       Date:  1964-12       Impact factor: 5.284

2.  Split-hand with unusual complications.

Authors:  J B GRAHAM; C E BADGLEY
Journal:  Am J Hum Genet       Date:  1955-03       Impact factor: 11.025

3.  Congenital scalp defects with distal limb anomalies: report of a family.

Authors:  B K Burton; L Hauser; H L Nadler
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

4.  The genetics of hand malformations.

Authors:  S A Temtamy; V A McKusick
Journal:  Birth Defects Orig Artic Ser       Date:  1978

5.  Split-hand and split-foot deformity inherited as an autosomal recessive trait.

Authors:  I C Verma; R Joseph; S Bhargava; S Mehta
Journal:  Clin Genet       Date:  1976-01       Impact factor: 4.438

6.  [Split hand and foot with familial occurrence].

Authors:  H NEUGEBAUER
Journal:  Z Orthop Ihre Grenzgeb       Date:  1962-04

7.  Observations on the human group system Lewis.

Authors:  R GRUBB
Journal:  Acta Pathol Microbiol Scand       Date:  1951

8.  Dominant ectrodactyly and possible germinal mosaicism.

Authors:  T J David
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

9.  A recessive form of ectrodactyly, and its implications in genetic counseling.

Authors:  A Freire-Maia
Journal:  J Hered       Date:  1971 Jan-Feb       Impact factor: 2.645

10.  The developmental field concept.

Authors:  J M Opitz
Journal:  Am J Med Genet       Date:  1985-05
View more
  7 in total

1.  Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.

Authors:  P Ianakiev; M W Kilpatrick; I Toudjarska; D Basel; P Beighton; P Tsipouras
Journal:  Am J Hum Genet       Date:  2000-06-05       Impact factor: 11.025

2.  Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.

Authors:  R S Ozen; B E Baysal; B Devlin; J E Farr; M Gorry; G D Ehrlich; C W Richard
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

Review 3.  Genomic imprinting: review and relevance to human diseases.

Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

4.  Heterogeneity of the autosomal dominant split hand/split foot malformation.

Authors:  J Zlotogora
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

5.  Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation.

Authors:  Mingzhu Miao; Shoulian Lu; Xiao Sun; Meng Zhao; Jue Wang; Xiaotan Su; Bai Jin; Lizhou Sun
Journal:  BMC Med Genomics       Date:  2022-07-13       Impact factor: 3.622

6.  Next generation sequencing of chromosomal rearrangements in patients with split-hand/split-foot malformation provides evidence for DYNC1I1 exonic enhancers of DLX5/6 expression in humans.

Authors:  Hana Lango Allen; Richard Caswell; Weijia Xie; Xiao Xu; Christopher Wragg; Peter D Turnpenny; Claire L S Turner; Michael N Weedon; Sian Ellard
Journal:  J Med Genet       Date:  2014-01-23       Impact factor: 6.318

7.  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

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.