📂 Diseases
spinocerebellar ataxia type 26 — Definition
Spinocerebellar ataksi tip 26 / spinocerebellar ataxia type 26
Spinocerebels are a qualitative neurodegenerative disease, which is rare in the form of a octane species 26,. The disease leads to balance, coordination and walking disorders as a result of damage to the brain (serebellum) and ile. The clinically late starter (usually after 40 years) is characterized by walking axie, speech disorder (dizartri) and eye movements abnormalities. Genetically associated with mutations in the EEF2 gene, and the disease combines.
Frequently Asked Questions
❓ What is Spinocerebellar ataksi tip 26?
Spinocerebellar ataksi tip 26; spinocerebels are a qualitative neurodegenerative disease, which is rare in the form of a octane species 26,. The disease leads to balance, coordination and walking disorders as a result of damage to the brain (serebellum) and ile. The clinically late starter (usually after 40 years) is characterized by walking axie, speech disorder (dizartri) and eye movements abnormalities. Genetically associated with mutations in the EEF2 gene, and the disease combines.
❓ What is spinocerebellar ataxia type 26 in Turkish?
The Turkish equivalent of "spinocerebellar ataxia type 26" is Spinocerebellar ataksi tip 26.
❓ Which medical field is Spinocerebellar ataksi tip 26 related to?
This term belongs to the Diseases category.