Análise de fatores genéticos associados ao desenvolvimento da síndrome metabólica durante a terapia com glicocorticoide em pacientes portadores da deficiência da 21-hidroxilase

Análise de fatores genéticos associados ao desenvolvimento da síndrome metabólica durante a terapia com glicocorticoide em pacientes portadores da deficiência da 21-hidroxilase

Introdução: A deficiência da 21-hidroxilase (21-OHD) é um frequente erro herdado do metabolismo que resulta no comprometimento da síntese do cortisol e/ou aldosterona e aumento da produção de andrógenos. A doença é caracterizada por uma diversidade fenotípica, variando desde virilização pré-natal da...

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Bibliographic Details
Main Author:	Moreira, Ricardo Paranhos Pires
Other Authors:	Bachega, Tânia Aparecida Sartori Sanchez
Format:	Others
Language:	pt
Published:	Biblioteca Digitais de Teses e Dissertações da USP 2014
Subjects:	11 beta-hydroxysteroid dehydrogenase type 1 11 Betahidroxiesteróide desidrogenase tipo 1 Congenital adrenal hyperplasia Glucocorticoid receptor Glucocorticoides Hiperplasia suprarrenal congênita lucocorticoids Metabolic syndrome Obesidade Obesity Polimorfismo genético Polymorphism Receptor de glucocorticoides Síndrome metabólica
Online Access:	http://www.teses.usp.br/teses/disponiveis/5/5166/tde-01042016-161323/

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