Authors: H. Obluková; H. Bučková Authors‘ workplace: Dětské kožní oddělení, Fakultní nemocnice Brno primářka MUDr. H. Bučková, PhD. Published in: Čes-slov Derm, , 2002, No. 3, p. 118-120 Category:
Waardenburg's Syndrome is a rare autosomal dominant hereditary disease characterized by different grades of impaired hearing, change in slon and hair pigmentation, a typical physiognomy. The authors describe the tase of a 5-year-old female patient with typical manifestations of Waardenburg's Syndrome type I. Symptoms of the disease of different intensity are found also in some of the maternal relatives.
Key words: genodermatoses - Waardenburg's
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