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Incomplete penetrance of MITF gene c.943C>T mutation in an extended family with Waardenburg syndrome type II.
Alehabib, Elham; Alinaghi, Somayeh; Pourfatemi, Fatemeh; Darvish, Hossein.
Afiliação
  • Alehabib E; Student Research Committee, Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, 1090, Vienna, Austria.
  • Alinaghi S; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Pourfatemi F; Sari Genetic Counseling Center, Welfare Office, Mazandaran, Iran.
  • Darvish H; Cancer Research Center, Semnan University of Medical Sciences, Semnan, Iran; Department of Medical Genetics, Semnan University of Medical Sciences, Semnan, Iran. Electronic address: darvish_mg@sbmu.ac.ir.
Int J Pediatr Otorhinolaryngol ; 135: 110014, 2020 Aug.
Article em En | MEDLINE | ID: mdl-32422366
Waardenburg syndrome (WS) is a group of genetic disorders that often determined by abnormal pigmentation and hearing impairment. Four subgroups of disease are recognized according to physical characteristics and involved genes. Mutation in the genes, MITF, SOX10, SNAI2, PAX3, KIT and KITLG are related to Waardenburg syndrome type II. In this study, we performed exome sequencing in a WS2 proband and detected a heterozygous non-sense variation in MITF. Clinical features, pedigrees investigations and molecular segregation revealed autosomal dominant inheritance with incomplete penetrance. To our knowledge it's the first evidence about incomplete penetrance of WS2 related to MITF gene.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Waardenburg / Códon sem Sentido / Penetrância / Fator de Transcrição Associado à Microftalmia Limite: Female / Humans / Male Idioma: En Revista: Int J Pediatr Otorhinolaryngol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Waardenburg / Códon sem Sentido / Penetrância / Fator de Transcrição Associado à Microftalmia Limite: Female / Humans / Male Idioma: En Revista: Int J Pediatr Otorhinolaryngol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Áustria