Kisho

Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy

epilepsy, familial adult myoclonic - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

epilepsy, familial adult myoclonic

MONDO:0000160

Overview

An epilepsy syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities.

OnsetADULT

ResearchLimited published research (4 articles)

Diagnosis

Biomarker and diagnostic research for epilepsy, familial adult myoclonic has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for epilepsy, familial adult myoclonic.

4 publications have been identified in PubMed for epilepsy, familial adult myoclonic. Research spans Basic Science / Preclinical (50%), Diagnostic / Biomarker (25%), and Clinical Trial Publication (25%).

Recent Publications

Coppola A (2025). [PMID: 39533755](https://pubmed.ncbi.nlm.nih.gov/39533755/). *Epilepsia open*. [Clinical Trial Publication]
Kühnel T (2025). [PMID: 40200849](https://pubmed.ncbi.nlm.nih.gov/40200849/). *Movement disorders : official journal of the Movement Disorder Society*. [Basic Science / Preclinical]
Ishiura H (2025). [PMID: 40571639](https://pubmed.ncbi.nlm.nih.gov/40571639/). *Rinsho shinkeigaku = Clinical neurology*. [Basic Science / Preclinical]
Urabe H (2025). [PMID: 41219789](https://pubmed.ncbi.nlm.nih.gov/41219789/). *BMC medical genomics*. [Diagnostic / Biomarker]

Data assembled from 2 of 12 sources · Last updated Oct 3, 2026, 9:34 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

← Back to All Diseases

epilepsy, familial adult myoclonic

Overview

Diagnosis

Research Landscape

Recent Publications

Medical References

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team