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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... |
