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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| Outros Autores: | , , , , , , |
| Formato: | article |
| Idioma: | por |
| Publicado em: |
2011
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| Assuntos: | |
| Texto completo: | http://hdl.handle.net/10400.4/1017 |
| País: | Portugal |
| Oai: | oai:rihuc.huc.min-saude.pt:10400.4/1017 |