Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/42713
Title: 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
Other Titles: Insuficiência adrenal leve causada por mutação do gene NR0B1 (DAX1) em menino com uma associação de hipogonadismo hipogonadotrófico, baixa estatura final e transtorno de déficit de atenção
Authors: Calliari, Luis Eduardo Procopio [UNIFESP]
Rocha, Milene N.
Monte, Osmar
Longui, Carlos Alberto
Universidade Federal de São Paulo (UNIFESP)
FCMSCSP
Issue Date: 1-Oct-2013
Publisher: Sbem-soc Brasil Endocrinologia & Metabologia
Citation: Arquivos Brasileiros De Endocrinologia E Metabologia. Rio De Janeiro, Rj: Sbem-soc Brasil Endocrinologia & Metabologia, v. 57, n. 7, p. 562-565, 2013.
Abstract: 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.
URI: http://repositorio.unifesp.br/11600/42713
ISSN: 0004-2730
Other Identifiers: http://dx.doi.org/10.1590/S0004-27302013000700011
Appears in Collections:Artigo

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