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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...

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