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AB044. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
BACKGROUND: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21OHD-CAH) is an autosomal recessive disorder. Around 95% of CAH cases are caused by deficiency of the enzyme 21-OH. CYP21A2 gene located on the short arm of chromosome 6 (6p21.3) encodes the protein enzyme 21-OH. METHODS:...
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| Publicat a: | Ann Transl Med |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
AME Publishing Company
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5641735/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s044 |
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