Spinocerebellar ataxia type 1 - Wikipedia
网页Spinocerebellar ataxia type 1 (SCA1) is a rare autosomal dominant disorder, which, like other spinocerebellar ataxias, is characterized by neurological symptoms including dysarthria, hypermetric saccades, and ataxia of gait and stance. This cerebellar dysfunction is progressive and permanent.
Spinocerebellar ataxia type 1 | About the Disease | GARD
网页Spinocerebellar ataxia type 1 (SCA1) is a progressive movement disorder that typically begins in early adulthood (but can affect children and older adults as well). Early signs and symptoms includes problems with coordination and balance (ataxia), speech and swallowing difficulties, muscle stiffness, and weakness in the muscles that control eye ...
Spinocerebellar Ataxia Type 1 - GeneReviews® - NCBI Bookshelf
网页1998年10月1日 · Spinocerebellar ataxia type 1 (SCA1) is characterized by progressive cerebellar ataxia, dysarthria, and eventual deterioration of bulbar functions. Early in the disease, affected individuals may have gait disturbance, slurred speech, difficulty with balance, brisk deep tendon reflexes, hypermetric saccades, nystagmus, and mild …
Spinocerebellar Ataxia (SCA): Symptoms, Causes & Types - Cleveland Clinic
网页What are the spinocerebellar ataxia types? Experts have discovered more than 40 types of SCAs so far, and that number may increase. They identify types by number (for example, spinocerebellar ataxia type 1, spinocerebellar ataxia type 2 and so on). All types of SCAs have similar causes and symptoms.
Spinocerebellar ataxia type 1 - MedlinePlus
网页Spinocerebellar ataxia type 1 (SCA1) is a condition characterized by progressive problems with movement. Explore symptoms, inheritance, genetics of this condition.
网页What is Spinocerebellar Ataxia Type 1? Spinocerebellar Ataxia type 1 (SCA1) is one specific type of Ataxia among a group of inherited diseases of the central nervous system. In SCA1, genetic defects lead to impairment of specific nerve fibers carrying messages to and from the brain resulting in
Spinocerebellar Ataxia - StatPearls - NCBI Bookshelf
网页2023年9月15日 · Spinocerebellar ataxia (SCA) is a progressive neurodegenerative inherited (autosomal dominant) heterogeneous disease that mainly affects the cerebellum. SCA is a subset of hereditary cerebellar ataxia and is a rare disease.
SCA1 - National Ataxia Foundation
网页SCA1 is one of the more common types of Spinocerebellar Ataxias. Approximately 1-2 in 100,000 people will develop SCA1, but the frequency varies considerably based on geographical location and ethnic background
Spinocerebellar ataxia type 1 - Orphanet
网页Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities.
Spinocerebellar Ataxias including Machado-Joseph Disease
网页The most common forms of SCA are types 1, 2, 3, and 6, which account for most of the disorders. SCA1 involves weakness and paralysis of the muscles of the eye and eyelid, blurred and double vision, and problems with moving the eyes.