Childhood Kidney Diseases
- Volume 1 Issue 1
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- Pages.91-96
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- 1997
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- 2384-0242(pISSN)
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- 2384-0250(eISSN)
Four Cases of Autosomal Recessive Polycystic Kidney Disease
상염색체 열성 다낭신 4례
- Choi Woong-Kyu (Department of Pediatrics, Seoul Paik Hospital, Inje University, College of Medicine) ;
- Lee Seung-Cheol (Department of Pediatrics, Seoul Paik Hospital, Inje University, College of Medicine) ;
- Park Yong-Won (Department of Pediatrics, Seoul Paik Hospital, Inje University, College of Medicine) ;
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Lee Chong-Guk
(Department of Pediatrics, Seoul Paik Hospital, Inje University, College of Medicine)
- 최웅규 (인제대학교 서울백병원 소아과학교실) ;
- 이승철 (인제대학교 서울백병원 소아과학교실) ;
- 박용원 (인제대학교 서울백병원 소아과학교실) ;
-
이종국
(인제대학교 서울백병원 소아과학교실)
- Published : 1997.05.01
Abstract
Polycystic kidney disease is defined as a heritable disorder with diffuse involvement of both kidneys without dysplasia other than cysts. The major clinical entities of autosomal recessive polycystic kidney disease and autosomal dominant polycystic kidney disease have a considerable overlap in clinical presentations and radiographic features in the pediatric population. We experienced three cases of autosomal recessive polycystic kidney disease of neonate who expired within 24 hours due to respiratory difficulty and the other case was detected by gross hematuria. So we report four cases with brief review of literatures.