An elderly patient with 17α-hydroxylase deficiency misdiagnosed as primary aldosteronism: a case report
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1472-6823
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
An elderly patient with 17α-hydroxylase deficiency misdiagnosed as primary aldosteronism: a case report ; volume:22 ; number:1 ; day:2 ; month:12 ; year:2022 ; pages:1-5 ; date:12.2022
BMC endocrine disorders ; 22, Heft 1 (2.12.2022), 1-5, 12.2022
- Creator
-
Ishinoda, Yuki
Uto, Asuka
Yamada, Yoshifumi
Okazaki, Maki
Asada, Hidetomo
Wakamatsu, Seina
Kurihara, Isao
Shibata, Hironori
Ishii, Tomohiro
Hasegawa, Tomonobu
Kumagai, Hiroo
Kasuga, Akira
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s12902-022-01216-y
- URN
-
urn:nbn:de:101:1-2023021321343452848948
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:53 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Ishinoda, Yuki
- Uto, Asuka
- Yamada, Yoshifumi
- Okazaki, Maki
- Asada, Hidetomo
- Wakamatsu, Seina
- Kurihara, Isao
- Shibata, Hironori
- Ishii, Tomohiro
- Hasegawa, Tomonobu
- Kumagai, Hiroo
- Kasuga, Akira
- SpringerLink (Online service)
Other Objects (12)
Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
Dopamine beta-hydroxylase deficiency
Hemmung der adrenalen 17α-Hydroxylase, 16α-Hydroxylase, 11β-Hydroxylase und 18-Hydroxylase beim Menschen durch Ketoconazol
Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population
17α-Hydroxylase [17alpha-Hydroxylase], 17,20-Lyase-Defizienz : eine systematische Übersichtsarbeit
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
An unusual presentation of tyrosine hydroxylase deficiency
17α-hydroxylase deficiency diagnosed in early infancy caused by a novel mutation of the CYP17A1 Gene17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene
POR polymorphisms are associated with 21 hydroxylase deficiency
Refractory hypokalemia with sexual dysplasia and infertility caused by 17α-hydroxylase deficiency and triple X syndrome: A case report
Flash glucose monitoring system was applied to cortisol treatment for a patient with congenital adrenal hyperplasia and 17α-hydroxylase deficiency
Primary aldosteronism in pregnancy
Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
Dopamine beta-hydroxylase deficiency
Hemmung der adrenalen 17α-Hydroxylase, 16α-Hydroxylase, 11β-Hydroxylase und 18-Hydroxylase beim Menschen durch Ketoconazol
Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population
17α-Hydroxylase [17alpha-Hydroxylase], 17,20-Lyase-Defizienz : eine systematische Übersichtsarbeit
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
An unusual presentation of tyrosine hydroxylase deficiency
17α-hydroxylase deficiency diagnosed in early infancy caused by a novel mutation of the CYP17A1 Gene17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene
POR polymorphisms are associated with 21 hydroxylase deficiency
Refractory hypokalemia with sexual dysplasia and infertility caused by 17α-hydroxylase deficiency and triple X syndrome: A case report
Flash glucose monitoring system was applied to cortisol treatment for a patient with congenital adrenal hyperplasia and 17α-hydroxylase deficiency
Primary aldosteronism in pregnancy
Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
Dopamine beta-hydroxylase deficiency
Hemmung der adrenalen 17α-Hydroxylase, 16α-Hydroxylase, 11β-Hydroxylase und 18-Hydroxylase beim Menschen durch Ketoconazol
Prevalence of CYP17A1 gene mutations in 17α-hydroxylase deficiency in the Chinese Han population
17α-Hydroxylase [17alpha-Hydroxylase], 17,20-Lyase-Defizienz : eine systematische Übersichtsarbeit
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
An unusual presentation of tyrosine hydroxylase deficiency
17α-hydroxylase deficiency diagnosed in early infancy caused by a novel mutation of the CYP17A1 Gene17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene
POR polymorphisms are associated with 21 hydroxylase deficiency
Refractory hypokalemia with sexual dysplasia and infertility caused by 17α-hydroxylase deficiency and triple X syndrome: A case report
Flash glucose monitoring system was applied to cortisol treatment for a patient with congenital adrenal hyperplasia and 17α-hydroxylase deficiency