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Original Article
A case of Holoprosencephaly.
Won Chil Lee, In Chae Kim, Kung Min Lee, Chull Zoo Jung, Wang Bok Lee
Clin Exp Pediatr. 1988;31(12):1674-1679.   Published online December 31, 1988
A case of Holoprosencephaly, alobar type in 1-day-old female infant was presented. This patient manifested median facial defects and had extracranial anomaly such as cardiac defects. Chromosome studies showed a normal female karyotype with 46 chromosomes. The diagnosis was confirmed by brain CT scan and autopsy. A brief review of literature was made.
Late Hemorrhagic Disease of Infancy.
Kwang Wook Ahn, Chull Zoo Jung, Hyo Seop Ju, Seung Woo Moon
Clin Exp Pediatr. 1986;29(6):679-683.   Published online June 30, 1986
Late hemorrhagic disease of infant is a hemorrhagic disease due to prothrombin complex deficiency from 1 week to 1 year of age. It is hypothesized that the bleeding occurring may have resulted from the simultaneous occurrence of two or three of the following factors: (1) interference with the intestinal production of vit K as a result of Antibiotic Agents, (2)...
Case Report
A Case of Osteogenesis Imperfecta.
Kwang Wook An, Chull Zoo Jung, Hyo Seop Joo, Seung Woo Moon
Clin Exp Pediatr. 1986;29(1):84-87.   Published online January 31, 1986
Osteogenesis imperfecta is an inherited disorders of connective tissue that affects the skeleton, ligament, sclera, and dentin. Characterized clinical manifestation are multiplefracture, blue sclera, deafness, joint laxity, thin skin, and odontogenesis imperfecta. We experienced acase of osteogenesis imperfecta in a one day old male newborn who chiefly complain respiratory distress, triangular shaped head and fracture and deformity of lower extremity....
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