Long-term follow-up of a female with congenital adrenal hyperplasia due to P450-oxidoreductase deficiency

P450 oxidoreductase deficiency (PORD) is a variant of congenital adrenal hyperplasia that is caused by POR gene mutations. The POR gene encodes a flavor protein that transfers electrons from nicotinamide adenine dinucleotide phosphate (NADPH) to all microsomal cytochrome P450 type II (including 21-h...

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Detalles Bibliográficos
Autores principales: Bonamichi, Beatriz D. S. F., Santiago, Stella L. M., Bertola, Débora R., Kim, Chong A., Alonso, Nivaldo, Mendonca, Berenice B., Bachega, Tania A. S. S., Gomes, Larissa G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Endocrinologia e Metabologia 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118638/
https://www.ncbi.nlm.nih.gov/pubmed/27737328
http://dx.doi.org/10.1590/2359-3997000000213

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118638/
https://www.ncbi.nlm.nih.gov/pubmed/27737328
http://dx.doi.org/10.1590/2359-3997000000213

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