医学
错义突变
外胚层发育不良
遗传学
少毛症
基因
机制(生物学)
病因学
疾病
皮肤病科
生物信息学
突变
病理
生物
哲学
认识论
出处
期刊:International Journal of Pediatrics
[Hindawi Publishing Corporation]
日期:2014-01-26
卷期号:41 (01): 64-66
标识
DOI:10.3760/cma.j.issn.1673-4408.2014.01.020
摘要
Clouston syndrome,also named hidrotic ectodermal dysplasia,is an autosomal dominant genetic disease.It is characterized by hypotrichosis,nail dystrophy and palmoplantar hyperkeratosis.It is caused by mutations in the GJB6 gene.Up to date,there are four GJB6 missense mutations that can cause Clouston syndrome:G1 1R,A88V,V37E and D50N.This article reviews the progress of gene diagnosis and pathogenic mechanism of Clouston syndrome,which can contribute to etiological diagnosis,genetic counseling,intervention as well as treatment.
Key words:
Clouston syndrome; Gene GJB6; Connexin 30; Gene diagnosis; Pathogenic mechanism
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