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17α-hydroxylase 결핍증에 의한 원발성 무월경 1예

Other Titles
 A Case of Primary Amenorrhea due to 17α-Hydroxylase Deficiency 
Authors
 안철우 
Citation
 Korean journal of Endocrine Surgery (대한내분비외과학회지), Vol.16(1) : 130~133, 2001 
Journal Title
 Korean journal of Endocrine Surgery (대한내분비외과학회지) 
ISSN
 1015-6380 
Issue Date
2001
Abstract
17α-Hydroxylase deficiency is a rare form of congenital adrenal hyperplasia that is characterized by primary amenorrhea, absence of secondary sex characteristics, hypertension, and a hypokalemic alkalosis that has resulted resulting from increased production of deoxycorticosterone and corticosterone by the adrenal. The diagnosis of this enzyme deficiency can be recognized by the increasing serum concentrations of steroid precursors, DOC and corticosterone and the decreasing concentrations of cortisol, and adrenal androgens. We diagnosed this in a 19 year old female who presented with primary amenorrhea. We report this case with a review of th literatures.
URI
http://ir.ymlib.yonsei.ac.kr/handle/22282913/142852
Appears in Collections:
1. 연구논문 > 1. College of Medicine > Dept. of Internal Medicine
Yonsei Authors
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