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Spinocerebellar ataxia
- Spinocerebellar ataxia type 36 (SCA36) is a condition characterized by progressive problems with movement that typically begin in mid-adulthood. People with this condition ...
- Spinocerebellar ataxia type 1 (SCA1) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with ...
- Spinocerebellar ataxia type 6 (SCA6) is a condition characterized by progressive problems with movement. People with this condition ... This phenomenon is called anticipation. SCA6 Type 6 spinocerebellar ataxia Genetic Testing Registry: Spinocerebellar ataxia type 6 Spinocerebellar ...
- Spinocerebellar ataxia type 3 (SCA3) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with ...
- Spinocerebellar ataxia type 2 (SCA2) is a condition characterized by progressive problems with movement. People with this condition ... be one of the most common types of spinocerebellar ataxia; however, all types of spinocerebellar ataxia are relatively ...
- Infantile-onset spinocerebellar ataxia (IOSCA) is a progressive disorder that affects the nervous system. Babies with IOSCA develop normally during the first ... hypacusis, and athetosis Genetic Testing Registry: Infantile onset ... Infantile-onset spinocerebellar ataxia Mitochondrial DNA depletion syndrome ...
- ... with ocular motor apraxia and hypoalbuminemia SCAN2 SCAR1 Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia, recessive, non-Friedreich type 1 Genetic Testing Registry: ...
- ... with hypogonadism and choroidal dystrophy syndrome Chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism Spinocerebellar ataxia, hypogonadotropic hypogonadism, and ...
- ... adulthood. This condition had previously been known as spinocerebellar ataxia with epilepsy (SCAE).The first symptom of MEMSA ... signs and symptoms of the condition. MEMSA SCAE Spinocerebellar ataxia with epilepsy Genetic Testing Registry: Spinocerebellar ataxia with ...
- ... TPP1 gene have also been found to cause spinocerebellar ataxia, autosomal recessive 7 (SCAR7), which is a condition ... Tests of TPP1 PubMed TRIPEPTIDYL PEPTIDASE I; TPP1 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7 NCBI Gene ClinVar Elleder ...
