This report describes a newborn with classical symptoms of cytomegalic inclusion disease at birth with hepatosplenomeglay, jaundice, hemolytic anemia, thrombocytopenia purpura and brain damage. The 24 years-old mother had a history of influenza-like disease at the 3 month gestation period. Complement-fixation antibody for cytomegalovirus were positive in the mother and newborn. He died on the first day of life. After the newborn's death, viral culture from the lung, liver grew cytomegalovirus. The significant histopathologic findings were inclusion-bearing cells were found in the lung, liver, kidney, lymph node, thyroid gland and pineal body as well as diffuse necrosis of the brain. We also discuss the maternal-fetal problems that can arise after infection by a cytomegalovirus.