Episodic ataxia (EA) is a neurological condition impairing movement. There are at least eight recognized types, which are all genetic but can have different ages of onset and symptoms. EA is rare ...

Episodic ataxia, characterised by periodic bouts of impaired coordination, imbalance and, in some cases, interictal ocular motor disturbances, is one such disorder. Ongoing research highlights ...

"Episodic ataxia 1 (EA1) is a movement disorder caused by inherited mutations in the human KCNA1 gene, which encodes Kv1.1, a voltage-gated potassium channel essential for normal function of the ...

Episodic ataxia – this is another rare type of hereditary ataxia. There are bouts or episodes of ataxia interspersed with normal periods with no ataxia. Bouts may last for minutes to hours.

DBMR has added a new report titled Episodic Ataxia Treatment Market with data Tables for historical and forecast years represented with Chats & Graphs spread through Pages with easy to understand ...

The findings provide a biological mechanism behind episodic ataxia 6, a rare neurological disorder. Episodic ataxia 6 is a debilitating illness that severely impacts balance and coordination and ...

This however does not cure the situation. For example in patients with episodic ataxia type 2, symptomatic relief may be obtained by treating with acetazolamide. Similarly ataxia with vitamin E ...

A provisional diagnosis of episodic ataxia type 2 was made in view of the patient's history of migraine, episodes of ataxia with normal examination between episodes and a strong family history.1, 2 ...

"Episodic Ataxia 1 (EA1) is a movement disorder caused by inherited mutations in the human KCNA1 gene, which encodes Kv1.1, a voltage-gated potassium channel essential for normal function of the ...

“Episodic Ataxia 1 (EA1) is a movement disorder caused by inherited mutations in the human KCNA1 gene, which encodes Kv1.1, a voltage-gated potassium channel essential for normal function of the ...