205 238

Cited 0 times in

17α-hydroxylase 결핍증에 의한 원발성 무월경 1예

Other Titles
 A Case of Primary Amenorrhea due to 17α-Hydroxylase Deficiency 
Authors
 임홍섭  ;  이선화  ;  홍종민  ;  남재현  ;  박희백  ;  안철우  ;  김도민  ;  임승길  ;  송영득  ;  이현철  ;  허갑범  ;  강인수 
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
https://ir.ymlib.yonsei.ac.kr/handle/22282913/142852
Files in This Item:
T200103159.pdf Download
Appears in Collections:
1. Journal Papers (연구논문) > 1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실)
Yonsei Authors
안철우(Ahn, Chul Woo)
Export
RIS (EndNote)
XLS (Excel)
XML
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse