Familial infantile myoclonic epilepsy

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Familial infantile myoclonic epilepsy

Synonyms: FIME | Familial infantile myoclonus epilepsy

A rare genetic infantile epilepsy syndrome disease characterized by neonatal- to infancy-onset myoclonic focal seizures occurring in various members of a family associated in some with mild dysarthria ataxia and borderline-to-moderate intellectual disability.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version October 2023.

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