Calliari LE

Calvari V

Carlos Alberto Longui

Correa RV

Darcan S

Guo W

Habiby RL

Luis Eduardo P. Calliari

Muscatelli F

Mylene N. Rocha

Nakae J

Osmar Monte

Perez Rodriguez O

Zanaria E

Arquivos brasileiros de Endocrinologia e Metabologia

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.</jats:p

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Arquivos Brasileiros de Endocrinologia & Metabologia

Mild adrenal insufficiency due to a NROB1 (DAX1) gene mutation in a boy presenting an association of hypogonadotropic hypogonadism, reduced final height and attention deficit disorder

Mild adrenal insufficiency due to a NROB1 (DAX1) gene mutation in a boy presenting an association of hypogonadotropic hypogonadism, reduced final height and attention deficit disorder

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