📂 Diseases
spinocerebellar ataxia type 13 — Definition
Spinocerebellar ataksi tip 13 / spinocerebellar ataxia type 13
Spinocerebels are a qualitative neurodegenerative disease with a pronounced, autosomal dominant transition. The disease leads to balance, coordination and walking disorders, depending on brain (serebellum) and the causative loss of nerve cells in the spinal cord. The clinical findings include slower progression, dysartri (conversion disorder) and oculomotor abnormalities. mutations in KCNC3 gene are the main genetic cause of this disease.
Frequently Asked Questions
❓ What is Spinocerebellar ataksi tip 13?
Spinocerebellar ataksi tip 13; spinocerebels are a qualitative neurodegenerative disease with a pronounced, autosomal dominant transition. The disease leads to balance, coordination and walking disorders, depending on brain (serebellum) and the causative loss of nerve cells in the spinal cord. The clinical findings include slower progression, dysartri (conversion disorder) and oculomotor abnormalities. mutations in KCNC3 gene are the main genetic cause of this disease.
❓ What is spinocerebellar ataxia type 13 in Turkish?
The Turkish equivalent of "spinocerebellar ataxia type 13" is Spinocerebellar ataksi tip 13.
❓ Which medical field is Spinocerebellar ataksi tip 13 related to?
This term belongs to the Diseases category.