U.S., June 14 -- ClinicalTrials.gov registry received information related to the study (NCT07019558) titled 'Ophthalmological Disorders in Dominant Spinal-cerebellar Ataxias' on May 28.
Brief Summary: Spinocerebellar ataxias (SCA) are rare genetic neurological disorders. The most common forms are SCA1, SCA2 and SCA3. Another more recently identified cause of ataxia is SCA27B.
These are progressive, incapacitating pathologies, with adult onset (generally between 30 and 60 years of age) and progressive involvement. They are characterized by gait instability (ataxia), coordination disorders (dysmetria) and speech disorders (dysarthria). A complex disorder may also be present, with impaired ocular motility, double vision (diplopia) and diffic...