📂 Diseases
spinocerebellar ataxia type 31 — Definition
Spinocerebellar ataksi tip 31 / spinocerebellar ataxia type 31
Spinocerebels are a neurodegenerative disease with autozomal dominant inheritance, which leads to aching loss of nerve cells in the brain and bronchi. The disease is characterized by walking strength, balance disorder and speech problems, usually starting in adulthood. Timely deterioration in muscle coordination, abnormalities and mild cognitive changes can also be seen in eye movements. SCA31 is specifically defined in Japan and is caused by a repeat mutation in the BEAN1 gene.
Frequently Asked Questions
❓ What is Spinocerebellar ataksi tip 31?
Spinocerebellar ataksi tip 31; spinocerebels are a neurodegenerative disease with autozomal dominant inheritance, which leads to aching loss of nerve cells in the brain and bronchi. The disease is characterized by walking strength, balance disorder and speech problems, usually starting in adulthood. Timely deterioration in muscle coordination, abnormalities and mild cognitive changes can also be seen in eye movements. SCA31 is specifically defined in Japan and is caused by a repeat mutation in the BEAN1 gene.
❓ What is spinocerebellar ataxia type 31 in Turkish?
The Turkish equivalent of "spinocerebellar ataxia type 31" is Spinocerebellar ataksi tip 31.
❓ Which medical field is Spinocerebellar ataksi tip 31 related to?
This term belongs to the Diseases category.