SCHMC

Laurence-Moon-Biedl 증후군 1례

Metadata Downloads
Alternative Title
A Case of Laurence-Moon-Biedl Syndrome
Abstract
Laurence-Moon-Biedl syndrome is an autosomal recessive disorder characterized by obesity, hypogenitalism, polydactyly, mental retardation and retinitis pigmentosa. Occasionally, this syndrome is accompanied by renal anomaly, nystagmus, cataract, syndactyly, microcephaly, oxycephaly and congenital heart disease. Recently, we have experienced a 8-year-old female patient who has retinitis pigmentosa, obesity, and polydactyly. We report a case of Laurence-Moon-Biedl syndrome with a review of literature.
All Author(s)
P. K. Jeon ; Y. H. Ohn ; J. O. Park ; C. H. Kim
Issued Date
2003
Type
Article
Keyword
Laurence-Moon-Biedl syndromeRetinitis pigmentosa
Publisher
대한소아소화기영양학회
The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
ISSN
1229-0114 ; 2093-5633
Citation Title
대한소아소화기영양학회지
Korean Journal of Pediatric Gastroenterology and Nutrition
Citation Volume
6
Citation Number
1
Citation Start Page
78
Citation End Page
83
Language(ISO)
kor
DOI
10.5223/kjpgn.2003.6.1.78
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/2954
Appears in Collections:
안과 > 1. Journal Papers
공개 및 라이선스
  • 공개 구분공개
파일 목록
  • 관련 파일이 존재하지 않습니다.

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