episodic kinesigenic dyskinesia 2

MeSH: C567026ORPHA: 98809

Contents

1. Overview
2. Available Treatments
3. Clinical Presentation
4. Classification & Codes

Overview

dystonia characterized by autosomal dominant inheritance of recurrent brief involuntary hyperkinesias triggered by sudden movements that has material basis in variation in the chromosome region 16q13-q22.1

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with episodic kinesigenic dyskinesia 2, sourced from HPO and Orphanet clinical annotations.

DystoniaChoreaAthetosisInvoluntary movementsDyskinesiaFocal sensory seizureSeizureMigraineWriter's cramp

Classification & Codes

MeSH Code

C567026

Orphanet Code

ORPHA:98809

episodic kinesigenic dyskinesia 2

MeSH	`C567026`
Orphanet	`ORPHA:98809`
Treatments	0 drug(s)
Symptoms on record	9 signs
Status	published

Factual Authority

Last Updated3/20/2026

Clinical DataHPO · Orphanet

Drug DataFDA · EMA · CDSCO