Literature DB >> 16199938

Variation in CASP10 gene is associated with idiopathic talipes equinovarus.

Amy L Heck1, Molly S Bray, Allison Scott, Susan H Blanton, Jacqueline T Hecht.   

Abstract

Idiopathic talipes equinovarus (ITEV), more commonly known as clubfoot, is a developmental deformity characterized by rigid ankle equinus, hindfoot varus, and forefoot adduction. This common birth defect is treatable, but the etiology of ITEV is largely unknown. Recently, a deletion in the chromosomal region 2q31-33 was found to be associated with clubfoot. Microsatellite markers spanning the region were genotyped in 57 multiplex ITEV families and 83 simplex trios. Family-based analysis revealed that two microsatellite markers, GATA149B10 and D2S1371, were associated with ITEV in the simplex trios. The 6cM region between the two markers contained the candidate genes CASP8, CASP10, and CFLAR. These genes encode proteins that are regulators of apoptosis, which is important during growth and development. Genotyping of SNPs throughout the genes in this sample of ITEV families has revealed positive linkage with association to the major allele of a variant in CASP10 in simplex ITEV white and Hispanic trios. This study is the first to find evidence for a candidate gene for ITEV and provides a scientific foundation to further explore the contributions of other apoptotic genes in the etiology of clubfoot.

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Year:  2005        PMID: 16199938     DOI: 10.1097/01.bpo.0000173248.96936.90

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  18 in total

1.  Variants in genes that encode muscle contractile proteins influence risk for isolated clubfoot.

Authors:  Katelyn S Weymouth; Susan H Blanton; Michael J Bamshad; Anita E Beck; Christine Alvarez; Steve Richards; Christina A Gurnett; Matthew B Dobbs; Douglas Barnes; Laura E Mitchell; Jacqueline T Hecht
Journal:  Am J Med Genet A       Date:  2011-08-10       Impact factor: 2.802

Review 2.  Update on clubfoot: etiology and treatment.

Authors:  Matthew B Dobbs; Christina A Gurnett
Journal:  Clin Orthop Relat Res       Date:  2009-02-18       Impact factor: 4.176

3.  Whole genome sequencing identifies ANXA3 and MTHFR mutations in a large family with an unknown equinus deformity associated genetic disorder.

Authors:  Zhiqun Zhang; Zhuqing Kong; Miao Zhu; Wenxiang Lu; Lei Ni; Yunfei Bai; Yue Lou
Journal:  Mol Biol Rep       Date:  2016-07-30       Impact factor: 2.316

4.  Joint hyperlaxity prevents relapses in clubfeet treated by Ponseti method-preliminary results.

Authors:  Dan Ionuţ Cosma; Andrei Corbu; Dan Viorel Nistor; Adrian Todor; Madalina Valeanu; Jose Morcuende; Sorin Man
Journal:  Int Orthop       Date:  2018-05-07       Impact factor: 3.075

5.  Studies of TBX4 and chromosome 17q23.1q23.2: an uncommon cause of nonsyndromic clubfoot.

Authors:  W Lu; C A Bacino; B S Richards; C Alvarez; J E VanderMeer; M Vella; N Ahituv; N Sikka; F R Dietz; S H Blanton; J T Hecht
Journal:  Am J Med Genet A       Date:  2012-06-07       Impact factor: 2.802

6.  Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.

Authors:  Audrey R Ester; Katelyn S Weymouth; Amber Burt; Carol A Wise; Allison Scott; Christina A Gurnett; Matthew B Dobbs; Susan H Blanton; Jacqueline T Hecht
Journal:  Am J Med Genet A       Date:  2009-12       Impact factor: 2.802

7.  Polygenic threshold model with sex dimorphism in clubfoot inheritance: the Carter effect.

Authors:  Lisa M Kruse; Matthew B Dobbs; Christina A Gurnett
Journal:  J Bone Joint Surg Am       Date:  2008-12       Impact factor: 5.284

8.  The developmental and genetic basis of 'clubfoot' in the peroneal muscular atrophy mutant mouse.

Authors:  J Martin Collinson; Nils O Lindström; Carlos Neves; Karen Wallace; Caroline Meharg; Rebecca H Charles; Zoe K Ross; Amy M Fraser; Ivan Mbogo; Kadri Oras; Masaru Nakamoto; Simon Barker; Suzanne Duce; Zosia Miedzybrodzka; Neil Vargesson
Journal:  Development       Date:  2018-02-08       Impact factor: 6.868

9.  Embryo with XYY syndrome presenting with clubfoot: a case report.

Authors:  Dimitrios Athanatos; Christos Tsakalidis; George P Tampakoudis; Maria N Papastergiou; Fillipos Tzevelekis; George Pados; Efstratios A Assimakopoulos
Journal:  Cases J       Date:  2009-09-01

10.  Variation in WNT7A is unlikely to be a cause of familial congenital talipes equinovarus.

Authors:  Guoqing Liu; Julie Inglis; Amanda Cardy; Duncan Shaw; Sukhy Sahota; Raoul Hennekam; Linda Sharp; Zosia Miedzybrodzka
Journal:  BMC Med Genet       Date:  2008-06-06       Impact factor: 2.103

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