Literature DB >> 32021595

Nonsyndromic Split-Hand/Foot Malformation: Recent Classification.

Muhammad Umair1,2,3, Amir Hayat4,5.   

Abstract

Split-hand/foot malformation (SHFM) is a genetic limb anomaly disturbing the central rays of the autopod. SHFM is a genetically heterogeneous disorder with variable expressivity inherited as syndromic and nonsyndromic forms. We provide an update of the clinical and molecular aspects of nonsyndromic SHFM. This rare condition is highly complex due to the clinical variability and irregular genetic inheritance observed in the affected individuals. Nonsyndromic SHFM types have been reviewed in terms of major molecular genetic alterations reported to date. This updated overview will assist researchers, scientists, and clinicians in making an appropriate molecular diagnosis, providing an accurate recurrence risk assessment, and developing a management plan.
Copyright © 2019 by S. Karger AG, Basel.

Entities:  

Keywords:  Ectrodactyly; Limb malformation; Recent classification; SHFM; Skeletal disorder

Year:  2019        PMID: 32021595      PMCID: PMC6997797          DOI: 10.1159/000502784

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  45 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

Review 2.  The Wnt signaling pathway in development and disease.

Authors:  Catriona Y Logan; Roel Nusse
Journal:  Annu Rev Cell Dev Biol       Date:  2004       Impact factor: 13.827

3.  A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.

Authors:  S Khan; S Basit; F K Zimri; N Ali; G Ali; M Ansar; W Ahmad
Journal:  Clin Genet       Date:  2011-05-27       Impact factor: 4.438

4.  Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients.

Authors:  Alison M Elliott; Jane A Evans
Journal:  Am J Med Genet A       Date:  2006-07-01       Impact factor: 2.802

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

Authors:  M Ahmad; H Abbas; S Haque; G Flatz
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

Review 6.  Pathogenesis of split-hand/split-foot malformation.

Authors:  Pascal H G Duijf; Hans van Bokhoven; Han G Brunner
Journal:  Hum Mol Genet       Date:  2003-04-01       Impact factor: 6.150

7.  A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly.

Authors:  Frances R Goodman; Frank Majewski; Amanda L Collins; Peter J Scambler
Journal:  Am J Hum Genet       Date:  2002-01-03       Impact factor: 11.025

Review 8.  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

9.  Mutagenesis Screen Identifies agtpbp1 and eps15L1 as Essential for T lymphocyte Development in Zebrafish.

Authors:  Christoph Seiler; Nichole Gebhart; Yong Zhang; Susan A Shinton; Yue-sheng Li; Nicola L Ross; Xingjun Liu; Qin Li; Alison N Bilbee; Gaurav K Varshney; Matthew C LaFave; Shawn M Burgess; Jorune Balciuniene; Darius Balciunas; Richard R Hardy; Dietmar J Kappes; David L Wiest; Jennifer Rhodes
Journal:  PLoS One       Date:  2015-07-10       Impact factor: 3.240

10.  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

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  2 in total

1.  Peripheral Nerve Innervation in Bilateral Cleft Hand Syndrome Elucidated by Ultrasound.

Authors:  Pietro Falco; Steven Hovius; Nens van Alfen
Journal:  Front Neurol       Date:  2022-05-20       Impact factor: 4.086

2.  SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably.

Authors:  Ewelina Bukowska-Olech; Anna Sowińska-Seidler; Jolanta Wierzba; Aleksander Jamsheer
Journal:  Orphanet J Rare Dis       Date:  2022-08-26       Impact factor: 4.303

  2 in total

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