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Syndrome in Question
Peruzzo, Juliano; Nazar, Fernanda Luca; Tubone, Mariana Quirino; Escobar, Gabriela Fortes; Cestari, Tania Ferreira.
  • Peruzzo, Juliano; Federal University of Rio Grande do Sul. Porto Alegre. BR
  • Nazar, Fernanda Luca; Federal University of Rio Grande do Sul. Porto Alegre. BR
  • Tubone, Mariana Quirino; Federal University of Rio Grande do Sul. Porto Alegre. BR
  • Escobar, Gabriela Fortes; Federal University of Rio Grande do Sul. Porto Alegre. BR
  • Cestari, Tania Ferreira; Federal University of Rio Grande do Sul. Porto Alegre. BR
An. bras. dermatol ; 90(4): 589-590, July-Aug. 2015. tab, ilus
Article in English | LILACS | ID: lil-759211
ABSTRACT
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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Full text: Available Index: LILACS (Americas) Main subject: Waardenburg Syndrome Type of study: Diagnostic study / Screening study Limits: Child / Female / Humans Language: English Journal: An. bras. dermatol Journal subject: Dermatology Year: 2015 Type: Article Affiliation country: Brazil Institution/Affiliation country: Federal University of Rio Grande do Sul/BR

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Full text: Available Index: LILACS (Americas) Main subject: Waardenburg Syndrome Type of study: Diagnostic study / Screening study Limits: Child / Female / Humans Language: English Journal: An. bras. dermatol Journal subject: Dermatology Year: 2015 Type: Article Affiliation country: Brazil Institution/Affiliation country: Federal University of Rio Grande do Sul/BR