Severe hypertension caused by 17α-hydroxylase deficiency: A case report

BACKGROUND: 17α-hydroxylase deficiency (17OHD) is an autosomal recessive genetic disease characterized by low renin hypertension, abnormal sexual development, and reduced androgen levels. The morbidity rate of 17OHD is less than 1/10,000, and a lack of knowledge of this condition may lead to misdiag...

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Detalles Bibliográficos
Autores principales: Zhao, YaJing, Wang, ChengYu, Guo, ZiHong, Yi, ChunXiu, Zhang, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036490/
https://www.ncbi.nlm.nih.gov/pubmed/36967917
http://dx.doi.org/10.1016/j.heliyon.2023.e14062

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036490/
https://www.ncbi.nlm.nih.gov/pubmed/36967917
http://dx.doi.org/10.1016/j.heliyon.2023.e14062

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