- Original Article
- Waardenburg's Syndrome in a Boy and Mother.
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D H Kim, M Y Kim, C S Suh, S Y Kim, J Y Jung
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Clin Exp Pediatr. 1988;31(5):655-659. Published online May 31, 1988
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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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