A young woman with hypogonadism, hypertension and hypokalaemia
The Medical Journal of Malaysia
;
: 242-3, 2009.
Article
in English
| WPRIM
| ID: wpr-630023
ABSTRACT
We report a case of a 16 years old girl who presented sequentially with primary amenorrhoea, hypertension and hypokalaemia. Eight years later, she was finally diagnosed with 17alpha-hydroxylase deficiency congenital adrenal hyperplasia. Previous antihypertensive medications were stopped. Hydrocortisone alone successfully maintained normotension and normokalaemia.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Steroid Hydroxylases
/
Adrenal Hyperplasia, Congenital
/
Diagnosis, Differential
/
Hypertension
/
Hypogonadism
/
Hypokalemia
Type of study:
Diagnostic study
Language:
English
Journal:
The Medical Journal of Malaysia
Year:
2009
Type:
Article
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