Abstract
WAARDENBURG SYNDROME TYPE I – A CASE SERIES FROM A SINGLE FAMILY
Dr. D. Manikyamba*, Dr. S. Chandra Sekhar, Dr. G. Sidhartha Kiran, Dr. K. T. V. Lakshman Kumar
ABSTRACT
Waardenburg syndrome is a rare autosomal dominantly inherited genetic disorder with non progressive audio pigmentary defect along with dystopia canthorum. The diagnosis is clinical and should be considered if an individual has 2 major or 1 major plus 2 minor criteria. In this article we report 9 cases of Waardenburg syndrome in a single family spread over 4 generations which include a pair of monozygotic twins.
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