SCA37 gene related symptoms and diseases

All the information presented here about the SCA37 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to SCA37 gene

Symptoms // Phenotype	% Cases
Ataxia	Very Common - Between 80% and 100% cases
Falls	Very Common - Between 80% and 100% cases
Limb dysmetria	Very Common - Between 80% and 100% cases
Diffuse cerebellar atrophy	Very Common - Between 80% and 100% cases
Scanning speech	Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with SCA37 gene alterations may also develop some of the following symptoms and phenotypes:

• Commonly - More than 50% cases

• Cogwheel rigidity
• Cerebellar vermis atrophy
• Dysdiadochokinesis
• Horizontal nystagmus
• Truncal ataxia
• Frequent falls
• Clumsiness
• Sensory impairment

And 15 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to SCA37 gene

Here you will find a list of rare diseases related to the SCA37. You can also use our tool to get a more accurate diagnosis based on your current symptoms.

Search interest in SCA37

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