Literature DB >> 17507202

Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation.

Hitoshi Osaka1, Ikuo Ogiwara, Emi Mazaki, Nami Okamura, Sumimasa Yamashita, Mizue Iai, Michiko Yamada, Kenji Kurosawa, Hiroko Iwamoto, Norio Yasui-Furukori, Sunao Kaneko, Tateki Fujiwara, Yushi Inoue, Kazuhiro Yamakawa.   

Abstract

We investigated the roles of mutations in voltage-gated sodium channel alpha 1 subunit gene (SCN1A) in epilepsies and psychiatric disorders. The SCN1A gene was screened for mutations in three unrelated Japanese families with generalized epilepsy with febrile seizure plus (GEFS+), febrile seizure with myoclonic seizures, or intractable childhood epilepsy with generalized tonic-clonic seizures (ICEGTC). In the family with GEFS+, one individual was affected with panic disorder and seizures, and another individual was diagnosed with Asperger syndrome and seizures. The novel mutation V1366I was found in all probands and patients with psychiatric disorders of the three families. These results suggest that SCN1A mutations may confer susceptibility to psychiatric disorders in addition to variable epileptic seizures. Unidentified modifiers may play critical roles in determining the ultimate phenotype of patients with sodium channel mutations.

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Year:  2007        PMID: 17507202     DOI: 10.1016/j.eplepsyres.2007.03.018

Source DB:  PubMed          Journal:  Epilepsy Res        ISSN: 0920-1211            Impact factor:   3.045


  10 in total

1.  Mapping genetic modifiers of survival in a mouse model of Dravet syndrome.

Authors:  A R Miller; N A Hawkins; C E McCollom; J A Kearney
Journal:  Genes Brain Behav       Date:  2013-11-14       Impact factor: 3.449

2.  Drosophila as a model for epilepsy: bss is a gain-of-function mutation in the para sodium channel gene that leads to seizures.

Authors:  Louise Parker; Miguel Padilla; Yuzhe Du; Ke Dong; Mark A Tanouye
Journal:  Genetics       Date:  2010-11-29       Impact factor: 4.562

3.  Fine mapping and candidate gene analysis of a dravet syndrome modifier locus on mouse chromosome 11.

Authors:  Jennifer A Kearney; Letonia D Copeland-Hardin; Samantha Duarte; Nicole A Zachwieja; Isaiah K Eckart-Frank; Nicole A Hawkins
Journal:  Mamm Genome       Date:  2022-05-23       Impact factor: 3.224

4.  Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalities.

Authors:  Melinda S Martin; Karoni Dutt; Ligia A Papale; Céline M Dubé; Stacey B Dutton; Georgius de Haan; Anupama Shankar; Sergio Tufik; Miriam H Meisler; Tallie Z Baram; Alan L Goldin; Andrew Escayg
Journal:  J Biol Chem       Date:  2010-01-25       Impact factor: 5.157

Review 5.  Genetics and function of neocortical GABAergic interneurons in neurodevelopmental disorders.

Authors:  E Rossignol
Journal:  Neural Plast       Date:  2011-08-18       Impact factor: 3.599

Review 6.  Antiepileptic Drug Discovery and Development: What Have We Learned and Where Are We Going?

Authors:  Aaron C Gerlach; Jeffrey L Krajewski
Journal:  Pharmaceuticals (Basel)       Date:  2010-09-01

7.  A psychiatric disease-related circular RNA controls synaptic gene expression and cognition.

Authors:  Amber J Zimmerman; Alexander K Hafez; Stephen K Amoah; Brian A Rodriguez; Michela Dell'Orco; Evelyn Lozano; Brigham J Hartley; Begüm Alural; Jasmin Lalonde; Praveen Chander; Maree J Webster; Roy H Perlis; Kristen J Brennand; Stephen J Haggarty; Jason Weick; Nora Perrone-Bizzozero; Jonathan L Brigman; Nikolaos Mellios
Journal:  Mol Psychiatry       Date:  2020-01-27       Impact factor: 15.992

Review 8.  Neurological Disorders and Risk of Arrhythmia.

Authors:  Joyce Bernardi; Kelly A Aromolaran; Ademuyiwa S Aromolaran
Journal:  Int J Mol Sci       Date:  2020-12-27       Impact factor: 5.923

9.  Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome.

Authors:  Anna Ka-Yee Kwong; Cheuk-Wing Fung; Siu-Yuen Chan; Virginia Chun-Nei Wong
Journal:  PLoS One       Date:  2012-07-25       Impact factor: 3.240

10.  Generalized epilepsy with febrile seizure plus (GEFS+) spectrum: Novel de novo mutation of SCN1A detected in a Malaysian patient.

Authors:  Emmilia H Tan; Abdul Aziz M Yusoff; Jafri M Abdullah; Salmi A Razak
Journal:  J Pediatr Neurosci       Date:  2012-05
  10 in total

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