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Apr 16, 2022 · Episodic ataxia is a genetic condition that causes problems with how you walk, move and balance. You experience these problems during episodes with a clear beginning and end. Episodic ataxia isn’t curable, but healthcare providers can help you manage symptoms with medications and physical therapy.
Sep 21, 2016 · Episodic ataxia (EA) is a clinically heterogeneous group of disorders that are characterized by recurrent spells of truncal ataxia and incoordination lasting minutes to hours. Most have an autosomal dominant inheritance pattern.
Episodic ataxia (EA) is an autosomal dominant disorder characterized by sporadic bouts of ataxia (severe discoordination) with or without myokymia (continuous muscle movement). There are seven types recognized but the majority are due to two recognized entities.
Jan 30, 2024 · There are eight recognized types of episodic ataxia. The types EA 1 and EA 2 are the most common. EA 1 involves brief bouts of ataxia that may last seconds or minutes.
Episodic ataxia is a group of related conditions that affect the nervous system and cause problems with movement and coordination. People with episodic ataxia have episodes of poor coordination and balance (ataxia).
Jan 15, 2019 · 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...
Episodic Ataxia is clinically characterized by attacks of Ataxia with a clear onset of resolution. There are now eight recognized episodic Ataxia syndromes, numbered 1-8, in addition to late-onset episodic Ataxia. The genes are known for EA1, EA2, ES5, and EA6.
Apr 22, 2024 · Episodic ataxia refers to a group of uncommon neurological conditions affecting coordination and balance. The types of episodic ataxia are distinguished by their symptoms and other factors. Episodes of uncontrollable muscle movements vary in length and frequency and may improve over time.
Jun 15, 2007 · Primary episodic ataxias are autosomal dominant channelopathies that manifest as attacks of imbalance and incoordination. Mutations in two genes, KCNA1 and CACNA1A, cause the best characterized and account for the majority of identified cases of episodic ataxia.
Mar 28, 2023 · Episodic ataxia (EA), characterized by recurrent attacks of cerebellar dysfunction, is the manifestation of a group of rare autosomal dominant inherited disorders. EA1 and EA2 are most frequently encountered, caused by mutations in KCNA1 and CACNA1A. EA3–8 are reported in rare families.
