Case Report: 17 Alpha-Hydroxylase Deficiency Masquerading as Primary Hyperaldosteronism

1990 ◽  
Vol 300 (6) ◽  
pp. 380-382 ◽  
Author(s):  
Daryl A. Cottrell ◽  
James M. Falko ◽  
Fernando A. Bello
Keyword(s):  
Case Report ◽  
Primary Hyperaldosteronism ◽  
Hydroxylase Deficiency

Hyporeninemic hypoaldosteronism with severe hyperkalemia following adrenalectomy for primary hyperaldosteronism : a case report

2014 ◽  
Author(s):  
Mikulas Pura ◽  
Jan Malina ◽  
Katarina Machalekova ◽  
Helena Imreova ◽  
Peter Kentos ◽  
...  
Keyword(s):  
Case Report ◽  
Primary Hyperaldosteronism ◽  
Severe Hyperkalemia

scholarly journals Primary hyperaldosteronism in childhood due to unilateral macronodular hyperplasia. Case report.

Hypertension ◽  
1984 ◽  
Vol 6 (1) ◽  
pp. 75-84 ◽  
Author(s):  
S E Oberfield ◽  
L S Levine ◽  
A Firpo ◽  
D Lawrence ◽  
E Stoner ◽  
...  
Keyword(s):  
Case Report ◽  
Primary Hyperaldosteronism

scholarly journals POS-443 AN UNUSUAL TREATMENT FOR 1,25 DIHYDROXY VITAMIN D3 - 24 HYDROXYLASE DEFICIENCY INDUCED HYPERCALCIURIA - CASE REPORT

2021 ◽  
Vol 6 (4) ◽  
pp. S192
Author(s):  
M.E. DUPUIS ◽  
S. Desmeules ◽  
P. Isenring ◽  
P. Douville ◽  
F. Mac-Way
Keyword(s):  
Case Report ◽  
Vitamin D3 ◽  
Hydroxylase Deficiency ◽  
1,25 Dihydroxy Vitamin D3

scholarly journals Rare combination of Turner syndrome and congenital adrenal hyperplasia with 21-hydroxylase deficiency: case report

2018 ◽  
Vol 64 (4) ◽  
pp. 432-436
Author(s):  
Ivana Ságová ◽  
Matej Stančík ◽  
Dušan Pávai ◽  
Daniela Kantárová ◽  
Anton Vaňuga ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Adrenal Hyperplasia ◽  
Hydroxylase Deficiency ◽  
Rare Combination ◽  
21 Hydroxylase Deficiency

scholarly journals Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report

2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Yukiko Mikami ◽  
Yasushi Takai ◽  
Mana Obata-Yasuoka ◽  
Ryo Kumagai ◽  
Hiroaki Yagyu ◽  
...  
Keyword(s):  
Case Report ◽  
Hydroxylase Deficiency

scholarly journals Splicing analysis of CYP11B1 mutation in a family affected with 11β-hydroxylase deficiency: case report

2016 ◽  
Vol 16 (1) ◽  
Author(s):  
Pattaranatcha Charnwichai ◽  
Patra Yeetong ◽  
Kanya Suphapeetiporn ◽  
Vichit Supornsilchai ◽  
Taninee Sahakitrungruang ◽  
...  
Keyword(s):  
Case Report ◽  
Hydroxylase Deficiency

scholarly journals 21-hydroxylase Deficiency Associated with Adrenal Tumor : Case Report of Two Brothers

1989 ◽  
Vol 65 (5) ◽  
pp. 525-536
Author(s):  
Yasushi SUNAGA ◽  
Mitsushige NISHIKAWA ◽  
Kiyoshi INABA ◽  
Noburo HIROZANE ◽  
Noboru INOUE ◽  
...  
Keyword(s):  
Case Report ◽  
Adrenal Tumor ◽  
Hydroxylase Deficiency ◽  
21 Hydroxylase Deficiency
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