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Intermediate lengths of the C9ORF72 hexanucleotide repeat expansion may synergistically contribute to attention deficit hyperactivity disorder in child and his father: case report.
Maj, Carlo; Chiarenza, Giuseppe Augusto; Faraone, Stephen V; Miriam, Ciani; Gennarelli, Massimo; Bonvicini, Cristian; Scassellati, Catia.
Afiliação
  • Maj C; Genetics Unit, IRCCS Istituto Centro San Giovanni Di Dio Fatebenefratelli, Brescia, Italy.
  • Chiarenza GA; Istitute for Genomic Statistics and Bioinformatics, Bonn, Germany.
  • Faraone SV; Department of Child and Adolescent Neuropsychiatry , Rho Hospital, Milan, Italy.
  • Miriam C; Department of Biomedicine, K.G. Jebsen Centre for Research on Neuropsychiatric Disorders, University of Bergen, Bergen, Norway; Department of Biomedicine, K.G. Jebsen Centre for Research on Neuropsychiatric Disorders, University of Bergen, Bergen, Norway.
  • Gennarelli M; Molecular Markers Laboratory, IRCCS Istituto Centro San Giovanni Di Dio Fatebenefratelli, Brescia, Italy.
  • Bonvicini C; Genetics Unit, IRCCS Istituto Centro San Giovanni Di Dio Fatebenefratelli, Brescia, Italy.
  • Scassellati C; Section of Biology and Genetic, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Neurocase ; 27(2): 138-146, 2021 04.
Article em En | MEDLINE | ID: mdl-33730968
ABSTRACT
We have summarized the abstract section as follows "We report a son and his father affected by Attention Deficit Hyperactivity Disorder (ADHD). They belonged to a larger cohort (116 ADHD children, 20 related parents, 77 controls) wholly genotyped forC9ORF72 expansion. Ten ADHD susceptibility genes were further investigated in the family. We revealed that son and father shared an intermediateC9ORF72 expansion and common variants inCDH23, ITGAE and MTRR. Bioinformatics highlighted aC9ORF72-MTRR interaction. This case-report underlines that in relatives with ADHD, carrying variants in ADHD susceptibility genes, the intermediateC9ORF72 repeats might have a potentially pathogenetic synergistic effect, supporting the multifactorial polygenic aetiopathogenetic profile of disease".
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Deficit de Atenção com Hiperatividade Limite: Child / Humans / Male Idioma: En Revista: Neurocase Assunto da revista: CIENCIAS DO COMPORTAMENTO / NEUROLOGIA / PSICOLOGIA / PSIQUIATRIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Deficit de Atenção com Hiperatividade Limite: Child / Humans / Male Idioma: En Revista: Neurocase Assunto da revista: CIENCIAS DO COMPORTAMENTO / NEUROLOGIA / PSICOLOGIA / PSIQUIATRIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Itália