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Recently defined epileptic encephalopathy related to WWOX gene mutation: six patients and new mutations.
Havali, Cengiz; Ekici, Arzu; Dorum, Sevil; Görükmez, Özlem; Topak, Ali.
Afiliación
  • Havali C; Department of Pediatrics, Division of Neurology, Bursa Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey.
  • Ekici A; Department of Pediatrics, Division of Neurology, Bursa Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey.
  • Dorum S; Department of Pediatrics, Division of Pediatric Metabolic Disorders, Bursa Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey.
  • Görükmez Ö; Department of Medical Genetics, Bursa Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey.
  • Topak A; Department of Medical Genetics, Bursa Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey.
Neurol Res ; 43(9): 744-750, 2021 Sep.
Article en En | MEDLINE | ID: mdl-34034642
Purpose: Pathogenic variants of the WWOX gene have been linked to sexual differentiation disorders, spinocerebellar ataxia, and epileptic encephalopathy (EE). We evaluated the clinical and molecular data from six newly diagnosed patients with WWOX-related EE.Methods: Clinical and molecular findings in six patients with EE were investigated, and biallelic pathogenic variants in the WWOX gene were identified. Clinical exome sequencing and Sanger sequencing were performed.Results: Three variations, as well as two novel mutations, in the WWOX gene were detected.Conclusion: Pathogenic WWOX mutations are associated with early-onset EE. Here, we report the case of six children with WWOX-related EE.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encefalopatías / Proteínas Supresoras de Tumor / Epilepsia / Oxidorreductasa que Contiene Dominios WW Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Neurol Res Año: 2021 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encefalopatías / Proteínas Supresoras de Tumor / Epilepsia / Oxidorreductasa que Contiene Dominios WW Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Neurol Res Año: 2021 Tipo del documento: Article País de afiliación: Turquía