Syndrome in Question

AbstractWaardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmentation changes and minor facial malformations. It has four clinical variants. We report the case of a girl who, like her mother, was affected by this syndrome. The diagnosis was made after detection and treatment of deafness.

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Bibliographic Details
Main Authors: Peruzzo,Juliano, Nazar,Fernanda Luca, Tubone,Mariana Quirino, Escobar,Gabriela Fortes, Cestari,Tania Ferreira
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Dermatologia 2015
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000400589
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