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De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability.
- Source :
-
European journal of human genetics : EJHG [Eur J Hum Genet] 2020 Jun; Vol. 28 (6), pp. 763-769. Date of Electronic Publication: 2020 Mar 10. - Publication Year :
- 2020
-
Abstract
- Previously, intragenic CAMTA1 copy number variants (CNVs) have been shown to cause non-progressive, congenital ataxia with or without intellectual disability (OMIM#614756). However, ataxia, intellectual disability, and dysmorphic features were all incompletely penetrant, even within families. Here, we describe four patients with de novo nonsense, frameshift or missense CAMTA1 variants. All four patients predominantly manifested features of ataxia and/or spasticity. Borderline intellectual disability and dysmorphic features were both present in one patient only, and other neurological and behavioural symptoms were variably present. Neurodevelopmental delay was found to be mild. Our findings indicate that also nonsense, frameshift and missense variants in CAMTA1 can cause a spastic ataxia syndrome as the main phenotype.
- Subjects :
- Ataxia pathology
Child
Child, Preschool
Female
Humans
Intellectual Disability pathology
Male
Muscle Spasticity pathology
Mutation
Phenotype
Syndrome
Young Adult
Ataxia genetics
Calcium-Binding Proteins genetics
Intellectual Disability genetics
Muscle Spasticity genetics
Trans-Activators genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1476-5438
- Volume :
- 28
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- European journal of human genetics : EJHG
- Publication Type :
- Academic Journal
- Accession number :
- 32157189
- Full Text :
- https://doi.org/10.1038/s41431-020-0600-5