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dc.contributor.authorStromme, P.en
dc.contributor.authorMangelsdorf, M.en
dc.contributor.authorScheffer, I.en
dc.contributor.authorGecz, J.en
dc.identifier.citationBrain & Development, 2002; 24(5):266-268en
dc.description.abstractClinical data from 50 mentally retarded (MR) males in nine X-linked MR families, syndromic and non-specific, with mutations (duplication, expansion, missense, and deletion mutations) in the Aristaless related homeobox gene, ARX, were analysed. Seizures were observed with all mutations and occurred in 29 patients, including one family with a novel myoclonic epilepsy syndrome associated with the missense mutation. Seventeen patients had infantile spasms. Other phenotypes included mild to moderate MR alone, or with combinations of dystonia, ataxia or autism. These data suggest that mutations in the ARX gene are important causes of MR, often associated with diverse neurological manifestations.en
dc.description.statementofresponsibilityStrømme, Petter ; Mangelsdorf, Marie E ; Scheffer, Ingrid E ; Gécz, Jozefen
dc.publisherElsevier Science BVen
dc.subjectX Chromosome; Humans; Epilepsies, Myoclonic; Spasms, Infantile; Seizures; Ataxia; Dystonia; Autistic Disorder; Phenotype; Mutation; Mutation, Missense; Genes, Homeobox; Infant; Male; Intellectual Disabilityen
dc.titleInfantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARXen
dc.typeJournal articleen
pubs.library.collectionPaediatrics publicationsen
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]en
Appears in Collections:Paediatrics publications

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