A novel mutation in CYP17A1 gene leads to congenital adrenal hyperplasia: A case report

BACKGROUND: Congenital adrenal hyperplasia is a rare autosomal recessive disorder where the mutation in P450 family 17 subfamily A member 1 gene (CYP17A1) is involved in its etiology. The disorder represents itself with low blood levels of estrogens, androgens, and cortisol that generally couples wi...

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Detalles Bibliográficos
Autores principales: Nazari, Majid, Yahya Vahidi Mehrjardi, Mohammad, Neghab, Nosrat, Aghabagheri, Mahdi, Ghasemi, Nasrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719517/
https://www.ncbi.nlm.nih.gov/pubmed/31508570
http://dx.doi.org/10.18502/ijrm.v17i6.4817

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719517/
https://www.ncbi.nlm.nih.gov/pubmed/31508570
http://dx.doi.org/10.18502/ijrm.v17i6.4817

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