Literature DB >> 12357471

Polydactyly: how many disorders and how many genes?

Leslie G Biesecker1.   

Abstract

Disorders that include polydactyly as a manifestation are diverse and numerous. Cataloging these disorders by phenotype and genotype demonstrates numerous overlapping phenotypes, genetic heterogeneity of phenotypes, and distinct phenotypes generated from mutations in single genes. To assess these issues, a list of disorders with polydactyly has been compiled from several sources. Among 119 disorders, 39 disorders are associated with mutations in genes, and among these, genotypic and phenotypic overlap is demonstrated. These issues highlight the need for a diagnostic system that catalogs both genotype and phenotype. Published 2002 Wiley-Liss, Inc.

Mesh:

Year:  2002        PMID: 12357471     DOI: 10.1002/ajmg.10779

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  12 in total

Review 1.  Polydactyly and genes.

Authors:  Shubha R Phadke; V H Sankar
Journal:  Indian J Pediatr       Date:  2010-02-22       Impact factor: 1.967

2.  Crossed polydactyly type I caused by a point mutation in the GLI3 gene in a large Chinese pedigree.

Authors:  Baowen Cheng; Yongli Dong; Li He; Wenru Tang; Haijing Yu; Jing Lu; Lin Xu; Bingrong Zheng; Kaiyuan Li; Chunjie Xiao
Journal:  J Clin Lab Anal       Date:  2006       Impact factor: 2.352

Review 3.  Polydactyly: how many disorders and how many genes? 2010 update.

Authors:  Leslie G Biesecker
Journal:  Dev Dyn       Date:  2011-03-28       Impact factor: 3.780

4.  Exome sequencing reveals a novel nonsense mutation of GLI3 in a Chinese family with 'non-syndromic' pre-axial polydactyly.

Authors:  Ying Xiang; Zhigang Wang; Jingxia Bian; Yunlan Xu; Qihua Fu
Journal:  J Hum Genet       Date:  2016-06-16       Impact factor: 3.172

Review 5.  What you can learn from one gene: GLI3.

Authors:  L G Biesecker
Journal:  J Med Genet       Date:  2006-06       Impact factor: 6.318

6.  Oral HRAS Mutation in Orofacial Nevus Sebaceous Syndrome (Schimmelpenning-Feuerstein-Mims-Syndrome): A Case Report With a Literature Survey.

Authors:  Reinhard E Friedrich; Martin Gosau; Andreas M Luebke; Christian Hagel; Felix K Kohlrusch; Michael Hahn; Simon VON Kroge; Jan Hahn; Ilse Wieland; Martin Zenker
Journal:  In Vivo       Date:  2022 Jan-Feb       Impact factor: 2.155

7.  Dissecting complex genetic interactions that influence the Engrailed-1 limb phenotype.

Authors:  Crystal L Murcia; Natalie A Bilovocky; Karl Herrup
Journal:  Mamm Genome       Date:  2004-05       Impact factor: 2.957

8.  Epidemiology, etiology, and genetic aspects of reduction deficiencies of the lower limb.

Authors:  Ismat Ghanem
Journal:  J Child Orthop       Date:  2008-04-09       Impact factor: 1.548

9.  A novel GLI3 mutation affecting the zinc finger domain leads to preaxial-postaxial polydactyly-syndactyly complex.

Authors:  Michael Volodarsky; Yshaia Langer; Ohad S Birk
Journal:  BMC Med Genet       Date:  2014-09-30       Impact factor: 2.103

Review 10.  The Greig cephalopolysyndactyly syndrome.

Authors:  Leslie G Biesecker
Journal:  Orphanet J Rare Dis       Date:  2008-04-24       Impact factor: 4.123

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