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Congenital Systemic Cytomegalic Inclusion Disease.

Journal of the Korean Pediatric Society 1990;33(1):100-106.
Published online January 31, 1990.
Congenital Systemic Cytomegalic Inclusion Disease.
Dong Beom Lee1, Dong Hyun Kim1, Jung Sik Min1, Chang Hee Choi1, Je Geun Chi2
1Department of Pediatrics, Seoul Adventist Hospital, Seoul, Korea
2Department of Pathology, College of Medicine, Seoul National University, Seoul, Korea
선천성 전신성 세포비대성 봉입체병
이동범1, 김동현1, 민정식1, 최창희1, 지제근2
1서울 위생병원 소아과
2서울대학교 의과대학 병리과학교실
Received: 10 September 1989   • Accepted: 10 September 1989
Abstract
The authors experienced a case of congenital systemic cytomegalic inclusion disease in a newborn baby. This case showed the clinical features of low birt wight (2,200 gm), numerous petechiae, severe jaundice, hepatosplenomegaly, hypotonia and respiratory difficulty with cyanosis and Apgar score of 3 at 1 minute at birth. In the clinical course, he showed hypotonia, repeated spell of apnea. These symptoms progressively worsened and he died 22 days after birth. The autopsy was performed and we found cytomegalovirus in cytoplasmic and intranuclear inclu- sion of tubular epithelial cells of kidney.
Key Words: Congenital Systemic Cytomegalic Inclusion Disease


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