A Retrospective Study of Hearing Loss in Patients Diagnosed with Peroxisome Biogenesis Disorders in the Zellweger Spectrum.

Lee, John; Yergeau, Christine; Kawai, Kosuke; Braverman, Nancy; Géléoc, Gwenaëlle S G

Lee, John; Yergeau, Christine; Kawai, Kosuke; Braverman, Nancy; Géléoc, Gwenaëlle S G.

Afiliação

Lee J; Department of Otolaryngology, Boston Children's Hospital, Center for Life Sciences, Boston, Massachusetts, USA.
Yergeau C; Department of Human Genetics/Department of Pediatrics, McGill University, Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Kawai K; Department of Otolaryngology, Boston Children's Hospital, Center for Life Sciences, Boston, Massachusetts, USA.
Braverman N; Department of Human Genetics/Department of Pediatrics, McGill University, Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Géléoc GSG; Department of Otolaryngology, Boston Children's Hospital, Center for Life Sciences, Boston, Massachusetts, USA.

Ear Hear ; 43(2): 582-591, 2022.

Article em En | MEDLINE | ID: mdl-34534157

Assuntos

Surdez; Perda Auditiva; Transtornos Peroxissômicos; Síndrome de Zellweger; Feminino; Humanos; Masculino; Estudos Retrospectivos; Síndrome de Zellweger/diagnóstico; Síndrome de Zellweger/metabolismo

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Zellweger / Transtornos Peroxissômicos / Surdez / Perda Auditiva Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Ear Hear Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

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