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Can diabetes cause cerebellar ataxia?

Can diabetes cause cerebellar ataxia?

Autoimmune cerebellar ataxia related to GAD-ab is a rare condition that typically affects women with late-onset type 1 diabetes or other autoimmune disorders.

Is diabetic neuropathy considered a neurological disease?

For example, diabetic amyotrophy causes pain, weakness and wasting of the thigh muscles, or cranial nerve… Diabetic neuropathy is a peripheral nerve disorder caused by diabetes or poor blood sugar control. The most common types of diabetic neuropathy result in problems with sensation in the feet.

What can be done about spinocerebellar ataxia 2?

Click on the title above to view this resource. Treatment of spinocerebellar ataxia 2 (SCA2) is supportive and aims to help the affected person maintain their independence and avoid injury.

Which is autosomal dominant spinocerebellar ataxia 2?

Spinocerebellar ataxia 2 (SCA2) is inherited in an autosomal dominant manner. This means that having one changed ( mutated) copy of ATXN2 (the responsible gene) in each cell is enough to cause signs and symptoms of the condition. [2]

How does the National Ataxia Foundation help people with ataxia?

The National Ataxia Foundation, a nonprofit organization dedicated to improving the lives of persons affected by ataxia, provides lists of neurologists, ataxia clinics, and movement disorder clinics. Research helps us better understand diseases and can lead to advances in diagnosis and treatment.

Is there a registry for patients with ataxia?

Coordination of Rare Diseases at Sanford (CoRDS) hosts a specific registry for patients with ataxia in partnership with the National Ataxia Foundation. The goal of the CoRDS registry is to connect as many patients and researchers as possible to help advance treatments and cures for rare diseases.

What are the symptoms of spinocerebellar ataxia type 2?

Collapse Section Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with coordination and balance (ataxia).

How is ataxia with axonal neuropathy type 2 inherited?

Spinocerebellar ataxia with axonal neuropathy type 2 is inherited in an autosomal recessive manner. This means that to be affected, a person must have a mutation in both copies of the responsible gene in each cell. Affected people inherit one mutated copy of the gene from each parent, who is referred to as a carrier.

When does cerebellar ataxia lead to neuropathy?

SCAN1 is characterized by late childhood-onset of a slowly progressive cerebellar ataxia, followed by areflexia and signs of peripheral neuropathy. Gaze nystagmus and cerebellar dysarthria usually develop after the onset of ataxic gait.

How is spinocerebellar ataxia 2 ( SCA2 ) inherited?

Inheritance Inheritance. Listen. Spinocerebellar ataxia 2 (SCA2) is inherited in an autosomal dominant manner. This means that having one changed (mutated) copy of ATXN2 (the responsible gene) in each cell is enough to cause signs and symptoms of the condition.