电荷综合征
后鼻孔闭锁
疣
色域
听力损失
表型
物候学
遗传学
医学
突变
生长迟缓
基因
生物
闭锁
儿科
听力学
内科学
解旋酶
怀孕
核糖核酸
作者
Carlos Javier Lobete Prieto,Isabel Rivas,Joaquín Fernández Toral,Pilar Madero Barrajón
出处
期刊:PubMed
[National Institutes of Health]
日期:2010-02-01
卷期号:108 (1): e9-e12
标识
DOI:10.1590/s0325-00752010000100016
摘要
The characteristic phenotype of CHARGE syndrome includes: coloboma, congenital heart defect, choanal atresia, retarded growth and development, genital abnormalities, ear anomalies with or without hearing loss, which give the name (an acronym) to this condition. The molecular cause in 60% of the cases are mutations in the chromodomain helicase DNAbinding protein gene (CHD7), with an estimated frequency of 1 in 10,000 live born infants. We describe 3, not related patients with a clinical diagnosis of CHARGE syndrome and each of them with a different mutation in the CHD7 gene sequence.
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