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A Case of Congenital Systemic Cytomegalic Inclusion Disease.

Journal of the Korean Pediatric Society 1990;33(2):220-224.
Published online February 28, 1990.
A Case of Congenital Systemic Cytomegalic Inclusion Disease.
Kong Sik Kim, Eun Young Kwak, Ho Seong Yoo, Sang Gi Park, Young Bong Park
Department of Pediatrics, College of Medicine, Chosun University, Kwang Ju, Korea
선천성 전신성 세포비대성 봉입체명 1례
김공식, 곽은영, 유호성, 박상기, 박영봉
조선대학교 의과대학 소아과학교실
Received: 8 May 1989   • Accepted: 11 October 1989
Abstract
We experienced a Case of Congenital Systemic Cytomegalic Inclusion Disease. A-50-day female infant was admitted to our hospital because of Jaundice. She was characterized by a microcephaly, microophalmia, corneal opacity, icteric sclera, hepatomegaly, and umbilical hernia. Diagnosis was confirmed by TORCH complex Ab study and liver biopsy. TORCH complex Ab study showed CMV IgG and IgM positive. The liver biopsy finding showed numerous hepatocyte with intranuclear inclusion body.
Key Words: Cytomegalic Inclusion Disease


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