What helps spinocerebellar ataxia?
The most common symptom of SCA is ataxia (a condition in which coordination and balance are affected). Physical therapy can help strengthen muscles, while special devices (e.g., cane, crutches, walker, or wheelchair) can assist in mobility and other activities of daily life.
What SCA 29?
Spinocerebellar ataxia type 29 (SCA29) is an autosomal dominant, non-progressive cerebellar ataxia characterized by infantile-onset hypotonia, gross motor delay and cognitive impairment. Affected individuals exhibit cerebellar dysfunction and often have cerebellar atrophy on neuroimaging.
What does spinocerebellar ataxia affect?
Ataxia is a degenerative disease affecting the nervous system, presenting poor coordination and movement, difficulties with speech, walking, fine motor skills, swallowing, and vision. It mainly affects people over 18 (adult-onset).
Why do individuals with spinocerebellar ataxia?
Inheritance. This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. An affected person usually inherits the altered gene from one affected parent . However, some people with SCA1 do not have a parent with the disorder.
How can I help my child with ataxia?
How Is Ataxic Cerebral Palsy Treated?
- physical therapy, occupational therapy, and speech therapy.
- leg braces, a walker, and/or a wheelchair.
- medicine for muscle pain or stiffness.
- special nutrition to help the child grow.
- surgery to improve movement in the legs, ankles, feet, hips, wrists, and arms.
How can I help someone with ataxia?
Other ataxia interventions include physical and occupational therapy, and adaptive devices such as a cane, walker or wheelchair. Patients with ataxia may benefit from regular physical and mental exercise, and eating healthy and sleeping well.
What is Gillespie syndrome?
Gillespie syndrome is a disorder that involves eye abnormalities, weak muscle tone from birth (congenital hypotonia), problems with balance and coordinating movements (ataxia), and mild to moderate intellectual disability.
How long can you live with cerebellar ataxia?
Life expectancy is generally shorter than normal for people with hereditary ataxia, although some people can live well into their 50s, 60s or beyond. In more severe cases, the condition can be fatal in childhood or early adulthood.
How fast does ataxia progress?
The age of onset and the rate of ataxia progression are perhaps the two most useful clinical features pointing to the cause. Rapid progression (within weeks to months) is characteristic of paraneoplastic spinocerebellar degeneration and sporadic Creutzfeldt-Jakob disease.