17α-hydroxylase/17,20-lyase deficiency in congenital adrenal hyperplasia: A case report

Congenital adrenal hyperplasia (CAH) is a rare autosomal recessive disorder caused by mutations in the cytochrome P450 family 17 subfamily A member 1 (CYP17A1) gene located on chromosome 10q24.3, which leads to a deficiency in 17α-hydroxylase/17,20-lyase. The disorder is characterized by low blood l...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Simiao, Hu, Shuhong, Yu, Xuefeng, Zhang, Muxun, Yang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355729/
https://www.ncbi.nlm.nih.gov/pubmed/27959413
http://dx.doi.org/10.3892/mmr.2016.6029

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355729/
https://www.ncbi.nlm.nih.gov/pubmed/27959413
http://dx.doi.org/10.3892/mmr.2016.6029

Ejemplares similares