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Original Article
Waardenburg's Syndrome in a Boy and Mother.
D H Kim, M Y Kim, C S Suh, S Y Kim, J Y Jung
Clin Exp Pediatr. 1988;31(5):655-659.   Published online May 31, 1988
Waardenburg's syndrome is a rare autosomal dominant disorder which is characterized by (1) lateral displacement of the medial canthi of the eyes and the inferior lacrimal puncta. (2) a broad, prominent root of the nose (3) hyperplasia of the medial portions of the eyebrows (4) white or grey forelock (5) partial or total heterochromia of the irides and (6) deaf-mutism. The authors experienced 2...
Three Cases of hereditary Spherocytosis.
D H Kim, M Y Kim, S Y Kim, J Y Jung
Clin Exp Pediatr. 1988;31(4):500-505.   Published online April 30, 1988
We experienced 3 cases of herediatry spherocytosis which occurred in a family. The family consited of parents, one sone and one daughter. The case I, Daughter showed the chief complaints of pallor ad generalized weakness. The case II, Son hoswed the chief complaint of jaundice. The case III, Father showed the chief complaints of fatigue and dizziness. Diagnosis was made by presence of spherocytes in...
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