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Ataxia is caused by a malfunction in the cerebellum.

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Ataxia is caused by a malfunction in the cerebellum.

Acquired Ataxia can be treated with medication or through surgery. It can be treated with exercises. There are various forms of the condition. Friedreich ataxia is the most common type. Affected individuals have a faulty gene in one or both sides of their genomes. It can be inherited from both parents, making it a hereditary condition. However, if the underlying cause is not found, it may be curable with medication.


The cause of ataxia will determine the treatment. The diagnosis of sporadic ataxia can be based on a family history of the disease. In rare cases, patients may be diagnosed with episodic ataxia and a specific gene mutation, such as POLG. A full diagnostic workup can help determine if there is a genetic disorder that causes ataxia. It is vital to note that there is currently no known cure for ataxia.


A family history of ataxia can be hereditary. The symptoms of hereditary ataxia may occur at birth or in adulthood. The severity of the condition depends on the type of ataxia and the type of mutation. For sporadic ataxia, the symptoms usually appear in adulthood and do not have a family history. The symptoms of ataxia may range from slurred speech to difficulty walking to severe cognitive impairment.



Source Link for study on ataxia- https://bit.ly/3qOaNRd

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