A Case of Nonsyndromic Intrahepatic Bile Duct Paucity with Congenital Bilateral Vocal Cord Paralysis and 13q Deletion

선천성 양측 성대마비와 13번 염색체 장완 결실이 동반된 비증후군성 간내담도부족증 1례

  • Chung, Ju-Young (Department of Pediatrics, College of Medicine, Inje University) ;
  • Lee, Jeong-Soo (Department of Pediatrics, College of Medicine, Inje University) ;
  • Kim, Byung-Eoi (Department of Pediatrics, College of Medicine, Inje University) ;
  • Choi, Myung-Jai (Department of Pediatrics, College of Medicine, Inje University) ;
  • Park, Dong-Chul (Department of Pediatrics, College of Medicine, Inje University) ;
  • Kim, Sang-Woo (Department of Pediatrics, College of Medicine, Inje University) ;
  • Kang, Kyung-Hoon (Department of Pathology, College of Medicine, Seoul National University)
  • 정주영 (인제대학교 의과대학 소아과학교실) ;
  • 이정수 (인제대학교 의과대학 소아과학교실) ;
  • 김병의 (인제대학교 의과대학 소아과학교실) ;
  • 최명재 (인제대학교 의과대학 소아과학교실) ;
  • 박동철 (인제대학교 의과대학 소아과학교실) ;
  • 김상우 (인제대학교 의과대학 소아과학교실) ;
  • 강경훈 (서울대학교 의과대학 병리학교실)
  • Received : 2001.03.10
  • Accepted : 2001.03.24
  • Published : 2001.04.30

Abstract

Nonsyndromic intrahepatic bile duct paucity is known to be associated with several kinds of etiology such as infection, chromosomal anomaly, metabolic disease and idiopathic. We report a rare case of intrahepatic bile duct paucity with congenital bilateral vocal cord paralysis and 13q deletion.

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