Calliari Luis Eduardo P, Rocha Mylene N, Monte Osmar, Longui Carlos Alberto
Arq Bras Endocrinol Metabol. 2013 Oct;57(7):562-5. doi: 10.1590/s0004-27302013000700011.
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.
NROB1(DAX1)基因突变可导致婴儿期肾上腺皮质功能不全的不同表型。这些患者的长期演变表明,可能与低促性腺激素性性腺功能减退有关。在本文中,我们描述了一名患有NROB1基因突变的患者的病情演变,该患者被诊断为轻度肾上腺皮质功能不全,除存在注意力缺陷障碍外,我们还强调了其低促性腺激素性性腺功能减退和身材矮小的情况。这些关联应使医生在对该疾病患者进行随访时予以关注。