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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... |