Deficiência da STAT5B: Uma nova síndrome de insensibilidade ao hormônio de crescimento associada a acometimento imunológico

2Citations
Citations of this article
N/AReaders
Mendeley users who have this article in their library.

Abstract

A new presentation of growth hormone insensitivity (GHI) caused by homozygous mutations in STAT5B (signal transducer and activator of transcription 5B) gene has been characterized in the last years. Its particularity is the association with severe immune dysfunction, especially with lymphocytic interstitial pneumonitis. This may mislead physicians into considering short stature as secondary to chronic immunological disease and consequently into underdiagnosing this form of GHI. The objective of this review is to propagate current knowledge about this rare pathology, facilitating the diagnosis of patients with GHI due to STAT5B mutations in endocrinology and other specialties clinics.

Cite

CITATION STYLE

APA

Scalco, R. C., Pugliese-Pires, P. N., & Jorge, A. A. L. (2013, July). Deficiência da STAT5B: Uma nova síndrome de insensibilidade ao hormônio de crescimento associada a acometimento imunológico. Arquivos Brasileiros de Endocrinologia e Metabologia. https://doi.org/10.1590/S0004-27302013000500001

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free