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Original Article
A Case of Congenital Systemic Cytomegalic Inclusion Disease.
Kong Sik Kim, Eun Young Kwak, Ho Seong Yoo, Sang Gi Park, Young Bong Park
Clin Exp Pediatr. 1990;33(2):220-224.   Published online February 28, 1990
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...
Congenital Systemic Cytomegalic Inclusion Disease.
Dong Beom Lee, Dong Hyun Kim, Jung Sik Min, Chang Hee Choi, Je Geun Chi
Clin Exp Pediatr. 1990;33(1):100-106.   Published online January 31, 1990
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...
Case Report
Congenital Systemic Cytomegalic Inclusion Disease: An Autopsy Case Report.
Seung Bok Cho, Boc Lyul Park, Mi Na Lee, Hea Soo Koo, Je Geun Chi
Clin Exp Pediatr. 1981;24(9):865-871.   Published online September 15, 1981
A case of systemic cytomegalovirus infection in a newborn baby is reported. This female baby was born after 36 weeks gestation to a 30 year-old mother who had no prenatal problem except for breech presentation and placenta previa for which Caesarian section was given. The mother has two healthy children. The clinical course of this baby was characterized by repeat...