Your browser doesn't support javascript.
loading
Targeted next-generation sequencing in the diagnosis of neurodevelopmental disorders.
Okamoto, N; Miya, F; Tsunoda, T; Kato, M; Saitoh, S; Yamasaki, M; Shimizu, A; Torii, C; Kanemura, Y; Kosaki, K.
Afiliação
  • Okamoto N; Department of Medical Genetics, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.
  • Miya F; Laboratory for Medical Science Mathematics, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
  • Tsunoda T; Laboratory for Medical Science Mathematics, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
  • Kato M; Department of Pediatrics, Yamagata University Faculty of Medicine, Yamagata, Japan.
  • Saitoh S; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Yamasaki M; Department of Pediatric Neurosurgery, Takatsuki General Hospital, Osaka, Japan.
  • Shimizu A; Division of Biomedical Information Analysis, Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Iwate, Japan.
  • Torii C; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
  • Kanemura Y; Division of Regenerative Medicine, Institute for Clinical Research, Osaka National Hospital, National Hospital Organization, Osaka, Japan.
  • Kosaki K; Department of Neurosurgery, Osaka National Hospital, National Hospital Organization, Osaka, Japan.
Clin Genet ; 88(3): 288-92, 2015 Sep.
Article em En | MEDLINE | ID: mdl-25156961
We developed a next-generation sequencing (NGS) based mutation screening strategy for neurodevelopmental diseases. Using this system, we screened 284 genes in 40 patients. Several novel mutations were discovered. Patient 1 had a novel mutation in ACTB. Her dysmorphic feature was mild for Baraitser-Winter syndrome. Patient 2 had a truncating mutation of DYRK1A. She lacked microcephaly, which was previously assumed to be a constant feature of DYRK1A loss of function. Patient 3 had a novel mutation in GABRD gene. She showed Rett syndrome like features. Patient 4 was diagnosed with Noonan syndrome with PTPN11 mutation. He showed complete agenesis of corpus callosum. We have discussed these novel findings.
Assuntos
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Sequenciamento de Nucleotídeos em Larga Escala / Transtornos do Neurodesenvolvimento Tipo de estudo: Diagnostic_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Clin Genet Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Sequenciamento de Nucleotídeos em Larga Escala / Transtornos do Neurodesenvolvimento Tipo de estudo: Diagnostic_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Clin Genet Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Japão