An elderly patient with 17α-hydroxylase deficiency misdiagnosed as primary aldosteronism: a case report

BACKGROUND: 17α-hydroxylase deficiency (17OHD) is a rare autosomal recessive disorder. Aldosterone levels are usually low in patients with 17OHD. However, among the approximately 150 cases of 17OHD reported to date, aldosterone levels were not low in all cases. Therefore, some 17OHD cases may have b...

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Detalles Bibliográficos
Autores principales: Ishinoda, Yuki, Uto, Asuka, Yamada, Yoshifumi, Okazaki, Maki, Asada, Hidetomo, Wakamatsu, Seina, Kurihara, Isao, Shibata, Hironori, Ishii, Tomohiro, Hasegawa, Tomonobu, Kumagai, Hiroo, Kasuga, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9717510/
https://www.ncbi.nlm.nih.gov/pubmed/36461073
http://dx.doi.org/10.1186/s12902-022-01216-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9717510/
https://www.ncbi.nlm.nih.gov/pubmed/36461073
http://dx.doi.org/10.1186/s12902-022-01216-y

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