Dubin-Johnson 증후군 1예

A Case of Dubin-Johnson Syndrome

  • 곽애정 (영남대학교 의과대학 소아과학교실) ;
  • 김미정 (영남대학교 의과대학 소아과학교실) ;
  • 조민정 (성삼병원) ;
  • 최광해 (영남대학교 의과대학 소아과학교실)
  • Kwak, Ae-Jung (Department of Pediatrics, College of Medicine, Yeungnam University) ;
  • Kim, Mi-Jung (Department of Pediatrics, College of Medicine, Yeungnam University) ;
  • Cho, Min-Jung (Sung Sam Hospital) ;
  • Choi, Kwang-Hae (Department of Pediatrics, College of Medicine, Yeungnam University)
  • 발행 : 2002.06.30

초록

저자들은 신생아시기에서부터 담즙정체성을 나타낸 Dubin-Johnson 증후군 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

Dubin-Johnson syndrome is a form of benign, familial idiopathic jaundice presenting with chronic intermittent conjugated hyperbilirubinemia and a melanin-like pigment has been found in the parenchymal liver cells. This disorder is rarely diagnosed in the neonatal period. We report a case of Dubin-Johnson syndrome presenting with neonatal cholestasis.

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