Literature DB >> 28127823

Mutational screening of GLI3, SHH, preZRS, and ZRS in 102 Chinese children with nonsyndromic polydactyly.

Ying Xiang1, Limin Jiang1, Bo Wang1, Yunlan Xu2, Haiqing Cai2, Qihua Fu1.   

Abstract

BACKGROUND: Polydactyly is a group of congenital limb malformations that show high degree of phenotypic variability and genetic heterogeneity.
RESULTS: In the present study, four genomic regions (exons of GLI3, SHH, and noncoding sequences of preZRS and ZRS) involved in hedgehog (Hh) signaling pathway were sequenced for 102 unrelated Chinese children with nonsyndromic polydactyly. Two GLI3 variants (c.2844 G > G/A; c.1486C > C/T) and four preZRS variants (chr7:156585336 A>G; chr7:156585421 C>A; chr7: 156585247 G>C; chr7:156585420 A > C) were observed in 2(2.0%) and 6(5.9%) patients, respectively. These variants are not over-represented in the Chinese healthy population. All the 8 cases showed preaxial polydactyly in hands. Additionally, no specific patterns of malformation predicted mutations in other candidate genes or sequences.
CONCLUSIONS: This is the first report of the assessment of the frequency of GLI3/SHH/preZRS/ZRS in Chinese patients to show any higher possibility of mutations or variants for the 4 genes or sequences in China. Developmental Dynamics 246:392-402, 2017.
© 2017 Wiley Periodicals, Inc. © 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  GLI3; SHH; ZRS; polydactyly; preZRS

Mesh:

Substances:

Year:  2017        PMID: 28127823     DOI: 10.1002/dvdy.24488

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  5 in total

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4.  Complex radial polydactyly in a Chinese family: inclusion of triphalangism, triplication, and syndactyly.

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5.  Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing.

Authors:  Bailing Zu; Xiaoqing Zhang; Yunlan Xu; Ying Xiang; Zhigang Wang; Haiqing Cai; Bo Wang; Guoling You; Qihua Fu
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  5 in total

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