Literature DB >> 7616545

Bilateral split hand/foot malformation and inv(7)(p22q21.3).

J M Cobben1, J B Verheij, W H Eisma, P H Robinson, R P Zwierstra, B Leegte, S Castedo.   

Abstract

A boy with typical tetramelic split hands and feet is described. In addition, there was a large arteriovenous malformation of the right arm. Chromosome studies showed a pericentric inversion of chromosome 7: 46,XY,inv(7)(p22q21.3). Inspection of the extremities and chromosome studies in the parents were normal. This case confirms the suggested localisation of a locus, important for early limb differentiation, on the long arm of chromosome 7, most probably in the chromosomal region 7q21.2-7q21.3. Previously reported cases are reviewed briefly.

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Year:  1995        PMID: 7616545      PMCID: PMC1050433          DOI: 10.1136/jmg.32.5.375

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  17 in total

1.  EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2-q21.3.

Authors:  M B Qumsiyeh
Journal:  Clin Genet       Date:  1992-08       Impact factor: 4.438

2.  Deletion of 7q22 and ectrodactyly.

Authors:  H Rivera; J Sanchez-Corona; V R Burgos-Fuentes; M J Melendez-Ruiz
Journal:  Genet Couns       Date:  1991

3.  Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3.

Authors:  S H Roberts; H E Hughes; S J Davies; A L Meredith
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

4.  Ectro-amelia syndrome associated with an interstitial deletion of 7q.

Authors:  M A Morey; R R Higgins
Journal:  Am J Med Genet       Date:  1990-01

5.  EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q11.21 and 9p12 (or 7p11.2 and 9q12) in three generations.

Authors:  T Hasegawa; Y Hasegawa; S Asamura; T Nagai; Y Tsuchiya; M Ninomiya; Y Fukushima
Journal:  Clin Genet       Date:  1991-09       Impact factor: 4.438

6.  Interstitial long-arm deletion of chromosome 7 and ectrodactyly.

Authors:  E H Tajara; M Varella-Garcia; A C Gusson
Journal:  Am J Med Genet       Date:  1989-02

7.  Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneity.

Authors:  F Gurrieri; M Genuardi; P Chiurazzi; G Gillessen-Kaesbach; G Neri
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

8.  Vascular abnormalities at the site of limb deficiency.

Authors:  B D Hall
Journal:  Am J Med Genet       Date:  1992-06-01

9.  Interstitial deletion of a chromosome 7 (q11.2q22.1) in a child with splithand/splitfoot malformation.

Authors:  R A Pfeiffer
Journal:  Ann Genet       Date:  1984

10.  Ectrodactyly of hands and feet in a child with a complex translocation including 7q21.2.

Authors:  M Sharland; M A Patton; L Hill
Journal:  Am J Med Genet       Date:  1991-06-15
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  7 in total

1.  Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report.

Authors:  Aswini Sivasankaran; Ambika Srikanth; Pooja S Kulshreshtha; Deenadayalu Anuradha; Jayarama S Kadandale; Chandra R Samuel
Journal:  Mol Syndromol       Date:  2016-02-03

2.  The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3.

Authors:  A Slavotinek; E Maher; P Gregory; P Rowlandson; S M Huson
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

3.  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

4.  Split hand/foot malformation due to chromosome 7q aberrations(SHFM1): additional support for functional haploinsufficiency as the causative mechanism.

Authors:  Anneke T van Silfhout; Peter C van den Akker; Trijnie Dijkhuizen; Joke B G M Verheij; Maran J W Olderode-Berends; Klaas Kok; Birgit Sikkema-Raddatz; Conny M A van Ravenswaaij-Arts
Journal:  Eur J Hum Genet       Date:  2009-04-29       Impact factor: 4.246

5.  Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3.

Authors:  J Ignatius; S Knuutila; S W Scherer; B Trask; J Kere
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

6.  Phenotypic subregions within the split-hand/foot malformation 1 locus.

Authors:  Malene B Rasmussen; Sven Kreiborg; Per Jensen; Mads Bak; Yuan Mang; Marianne Lodahl; Esben Budtz-Jørgensen; Niels Tommerup; Lisbeth Tranebjærg; Nanna D Rendtorff
Journal:  Hum Genet       Date:  2016-02-02       Impact factor: 4.132

Review 7.  Split hand/foot malformation genetics supports the chromosome 7 copy segregation mechanism for human limb development.

Authors:  Amar J S Klar
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2016-12-19       Impact factor: 6.237

  7 in total

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