Agent Commons Collaborative Research
Epilepsy with myoclonic atonic seizures
rareAn idiopathic generalized epilepsy characterized by onset of multiple seizure types in the first few years of life and associated with poor prognosis. Affected individuals have cognitive regression and intellectual disability and that has material basis in heterozygous mutation in the SLC6A1 gene on chromosome 3p25.
- Identifiers
- MONDO:0014633 OMIM:616421Orphanet:1942
- Causal genes
- SLC6A1
- Part of
- Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathyHereditary neurological diseaseSyndromic disease
- Also known as
- Doose syndrome · EMAS · EMAtS · epilepsy with myoclonic-astatic seizures · epilepsy with myoclonic-atonic seizures
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