Syndrome in Question
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Waardenburg 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.
Syndrome in Question, Dermatopatias genéticas, Doenças genéticas inatas, Dermatology, Deafness, Surdez, Genetic diseases, inborn, Early Diagnosis, Phenotype, Skin diseases, genetic, RL1-803, Síndrome de Waardenburg, Humans, Female, Waardenburg Syndrome, Child, Waardenburg syndrome
Syndrome in Question, Dermatopatias genéticas, Doenças genéticas inatas, Dermatology, Deafness, Surdez, Genetic diseases, inborn, Early Diagnosis, Phenotype, Skin diseases, genetic, RL1-803, Síndrome de Waardenburg, Humans, Female, Waardenburg Syndrome, Child, Waardenburg syndrome
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