Literature DB >> 3817811

X-chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindred.

M Ahmad, H Abbas, S Haque, G Flatz.   

Abstract

A Pakistani kindred comprising seven generations and 36 members with the split-hand/split-foot anomaly is described. The full expression of the trait, monodactylous or split hand and split foot, mainly of the lobster-claw type, was present in 33 males and 3 females. Other females showed a distinctly milder expression of the trait, usually in the form of partial syndactyly, metacarpal and phalangeal hypoplasia, and malformation. The distribution of the affected members in the pedigree is compatible with X-chromosomal inheritance. Hemizygous males and presumably homozygous females exhibit the typical split-hand/split-foot anomaly, whereas only a part of the obligatory heterozygous females show the milder expression. There were no associated anomalies, such as ectodermal dysplasia, cleft lip/palate, macular degeneration, malformations of the long bones or internal organs, and overt mental retardation.

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Mesh:

Year:  1987        PMID: 3817811     DOI: 10.1007/bf00591081

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  4 in total

1.  [Delayed mutation in man; a critical observation on the work of Ch. Auerbachs (1956)].

Authors:  F VOGEL
Journal:  Ann Hum Genet       Date:  1958-02       Impact factor: 1.670

2.  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

3.  Monodactylous splithand-splitfoot. A malformation occurring in three distinct genetic types.

Authors:  G Bujdoso; W Lenz
Journal:  Eur J Pediatr       Date:  1980-05       Impact factor: 3.183

4.  Familial occurrence of severe ulnar aplasia and lobster claw feet: a new syndrome.

Authors:  H van den Berghe; J Dequeker; J P Fryns; G David
Journal:  Hum Genet       Date:  1978-05-16       Impact factor: 4.132

  4 in total
  17 in total

1.  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.

Authors:  Mohammed Naveed; Swapan K Nath; Mathew Gaines; Mahmoud T Al-Ali; Najib Al-Khaja; David Hutchings; Jeffrey Golla; Samuel Deutsch; Armand Bottani; Stylianos E Antonarakis; Uppala Ratnamala; Uppala Radhakrishna
Journal:  Am J Hum Genet       Date:  2006-11-29       Impact factor: 11.025

2.  Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25.

Authors:  A Raas-Rothschild; S Manouvrier; M Gonzales; J P Farriaux; S Lyonnet; A Munnich
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

3.  Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation.

Authors:  Xue Wang; Qian Xin; Lin Li; Jiangxia Li; Changwu Zhang; Rongfang Qiu; Chenmin Qian; Hailing Zhao; Yongchao Liu; Shan Shan; Jie Dang; Xianli Bian; Changshun Shao; Yaoqin Gong; Qiji Liu
Journal:  Eur J Hum Genet       Date:  2014-02-05       Impact factor: 4.246

4.  Nonsyndromic Split-Hand/Foot Malformation: Recent Classification.

Authors:  Muhammad Umair; Amir Hayat
Journal:  Mol Syndromol       Date:  2019-09-18

5.  Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1.

Authors:  M Faiyaz ul Haque; S Uhlhaas; M Knapp; H Schüler; W Friedl; M Ahmad; P Propping
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

Review 6.  Cleft hand/foot: clinical and developmental aspects.

Authors:  P W Buss
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

7.  Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.

Authors:  S E Palmer; S W Scherer; M Kukolich; E M Wijsman; L C Tsui; K Stephens; J P Evans
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

8.  Familial ectrodactyly syndrome in a nigerian child: a case report.

Authors:  Mathew Durowaye; Muhammed Adeboye; Sefiyah Yahaya-Kongoila; Adeline Adaje; Omotayo Adesiyun; Samuel Kolade Ernest; Olugbenga Ayodeji Mokuolu; Abdulrasheed Adegboye
Journal:  Oman Med J       Date:  2011-07

9.  Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.

Authors:  Hiroki Kano; Kenji Kurosawa; Emiko Horii; Shiro Ikegawa; Hideki Yoshikawa; Hiroki Kurahashi; Tatsushi Toda
Journal:  Hum Genet       Date:  2005-10-19       Impact factor: 4.132

Review 10.  Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.

Authors:  S W Scherer; P Poorkaj; T Allen; J Kim; D Geshuri; M Nunes; S Soder; K Stephens; R A Pagon; M A Patton
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

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