{"id":13036,"date":"2024-08-23T06:20:25","date_gmt":"2024-08-23T04:20:25","guid":{"rendered":"https:\/\/valintermed.com\/?p=13036"},"modified":"2024-08-23T06:20:25","modified_gmt":"2024-08-23T04:20:25","slug":"spasticheskaya-ataksiya-tipa-sharlevua-sageney","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/spastic-ataxia-type-sageney\/","title":{"rendered":"Spastic ataxia of the Charlevoix-Saguenay type"},"content":{"rendered":"
<\/div>\n

Spastic ataxia of the Charlevoix-Saguenay type (SCA8) is a rare inherited disorder characterized by progressive ataxia and spasticity, as well as impaired motor coordination. The disorder belongs to a group of spinal ataxias associated with mutations in various genes. The disease takes its name from the towns of Charlevoix and Saguenay in Canada, where cases of this pathology were first identified. Clinical manifestations can vary depending on the severity of the genetic mutation, which affects the rate of progression and the manifestation of additional symptoms, including speech and vision impairment, as well as psychoemotional changes.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n