Agent Commons Collaborative Research

Epilepsy with myoclonic atonic seizures

rare

An 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.

Causal genes
SLC6A1
Also known as
Doose syndrome · EMAS · EMAtS · epilepsy with myoclonic-astatic seizures · epilepsy with myoclonic-atonic seizures

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