促性腺激素减退症
肾上腺功能不全
医学
身材矮小
儿科
突变
青春期延迟
疾病
原发性肾上腺功能不全
内科学
内分泌学
基因
遗传学
激素
生物
作者
Luís Eduardo Calliari,Mylene Neves Rocha,Osmar Monte,Carlos Alberto Longui
标识
DOI:10.1590/s0004-27302013000700011
摘要
Mutation on NROB1 (DAX1) gene can cause different phenotypes of adrenal insufficiency in infancy. Long-term evolution of these patients shows that it is possible to have an association with hypogonadotropic hypogonadism. In this article we describe the evolution of a patient with NROB1 gene mutation, diagnosed with a mild form of adrenal insufficiency, and we highlight the presence of hypogonadotropic hypogonadism and short stature, besides the presence of attention deficit disorder. Such associations should make physicians aware during the follow-up of patients with this disease.
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