Hiperplasia Congénita da Suprarrenal de Expressão Tardia por Deficiência de 21-Hidroxilase

The deficiency of the enzyme 21-hydroxylase (21-HO) is responsible for about 90% to 95% of all cases of congenital adrenal hyperplasia (HCSR). This disorder is one of the most frequent hereditary illnesses of autosomal recessive trait. The illness can be presented in two clinical forms: 1 - classic,...

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Bibliographic Details
Main Author: Vieira, A (author)
Other Authors: Paiva, S (author), Baptista, C (author), Ruas, L (author), Silva, J (author), Gonçalves, J (author), Carrilho, F (author), Carvalheiro, M (author)
Format: article
Language:por
Published: 2011
Subjects:
Hiperplasia Congénita da Supra-Renal
21-Hidroxilase
Online Access:http://hdl.handle.net/10400.4/1017
Country:Portugal
Oai:oai:rihuc.huc.min-saude.pt:10400.4/1017

Internet

http://hdl.handle.net/10400.4/1017

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