📂 Diseases
spinocerebellar ataxia type 19/22 — Definition
Spinocerebellar ataksi tip 19/22 / spinocerebellar ataxia type 19/22
Spinocerebels are a rare autosomal dominant qualitative neurodegenerative disease in the form of anataxis 19/22. The disease is characterized by nucleus loss of nerve cells in the brain (serebellum) and omurilik. Clinically, it manifests itself with findings such as balance and coordination disorder (ataxis), speech strength (dizartri) and abnormalities (nistagmus). The initial age and severity of the disease may vary between individuals.
Frequently Asked Questions
❓ What is Spinocerebellar ataksi tip 19/22?
Spinocerebellar ataksi tip 19/22; spinocerebels are a rare autosomal dominant qualitative neurodegenerative disease in the form of anataxis 19/22. The disease is characterized by nucleus loss of nerve cells in the brain (serebellum) and omurilik. Clinically, it manifests itself with findings such as balance and coordination disorder (ataxis), speech strength (dizartri) and abnormalities (nistagmus). The initial age and severity of the disease may vary between individuals.
❓ What is spinocerebellar ataxia type 19/22 in Turkish?
The Turkish equivalent of "spinocerebellar ataxia type 19/22" is Spinocerebellar ataksi tip 19/22.
❓ Which medical field is Spinocerebellar ataksi tip 19/22 related to?
This term belongs to the Diseases category.