Episodic Ataxia, Type 2 [Supplementary Concept]
The most common form of episodic ataxia, a genetically heterogeneous condition characterized by episodes of incoordiantion and imbalance similar to progressive ataxia. Episodic ataxia 2 exhibits autosomal dominant inheritance and is further characterized by onset in childhood or adolescence and the occurence of nystagmus, TINNITUS; MIGRAINE HEADACHE, and other neurologic symptoms. Episodes are often triggered by sudden movements, fatigue, stress, stimulant or alcohol use and may be treated by ACETAZOLAMIDE. Mutations in the CACNA1A gene have been identified. OMIM: 108500
Date introduced: August 25, 2010
MeSH Unique ID: C535506
Heading Mapped to:
Entry Terms:
- Nystagmus-associated episodic ataxia
- Episodic ataxia type 2
- Cerebellopathy, hereditary paroxysmal
- Ataxia, familial, paroxysmal
- Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia
- Acetazolamide-responsive episodic ataxia syndrome
- Cerebellar ataxia, paroxysmal, Acetazolamide-responsive
- Acetazolamide-Responsive Hereditary Paroxysmal Cerebellar Ataxia
- Ataxia, Episodic, With Nystagmus
- Ataxia, Familial Paroxysmal
- Episodic ataxia with nystagmus
- Episodic Ataxia, Nystagmus-Associated