A rare genetic epilepsy syndrome characterized by infantile or childhood onset of focal motor seizures remitting with age, as well as childhood onset of exercise-induced dystonia which often persists ...
Comprehensive, easy-to-understand information about this condition
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Organizations with approved therapies for this disease
No approved therapies yet
Research is ongoing — 1 company has orphan drug designations for this disease
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.
AI-curated news mentioning rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
Updated Feb 1, 2026
A case report details a patient with Rasmussen's encephalitis who experienced a decade of refractory epilepsy and hemispheric atrophy. This study contributes to the understanding of the disease's progression and potential treatment challenges.
Regla María Garci Espejo shares her personal story of growing up with a sister affected by West syndrome, a severe early-onset epilepsy. This narrative highlights the challenges faced by families dealing with rare diseases and aims to raise awareness.
CDC releases new data on epilepsy, highlighting demographic trends in adoption among men and women aged 18-44. The report aims to raise awareness about epilepsy and its impact on family dynamics.
A CDC study reveals that approximately 1% of adults have active epilepsy, with over one-third not receiving adequate treatment. This highlights the ongoing need for improved awareness and access to care for individuals with epilepsy.