Waardenburg's Syndrome
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:
Overview
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
Labels
Dermatology & STDs Paediatric dermatology & STDsArticle was published in
Czech-Slovak Dermatology
2002 Issue 3
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