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PMPCA autosomal recessive congenital cerebellar ataxia is a rare inherited brain disorder that mainly affects the cerebellum, the part of the brain that controls balance and...
Autosomal recessive congenital cerebellar ataxia due to PMPCA mutation is a genetic brain movement disorder that starts in infancy or early childhood. “Autosomal recessive” means a...
Autosomal recessive spinocerebellar ataxia 2 (SCAR2) is a rare, inherited brain disorder. It mainly affects the cerebellum, the part of the brain that controls balance and...
CWF19L1 – Autosomal Recessive Congenital Cerebellar Ataxia (SCAR17) is a rare, inherited brain disorder that starts in infancy or early childhood. It mainly affects the cerebellum,...
Autosomal Recessive Congenital Cerebellar Ataxia Caused by Mutation in CWF19L1 (SCAR17) is a rare, inherited brain disorder. It mainly affects the cerebellum, the part of the...
Autosomal recessive cerebellar ataxia due to CWF19-like cell cycle control factor 1 (CWF19L1) deficiency is a rare, inherited brain disorder that mainly affects the cerebellum, the...
Autosomal Recessive Spinocerebellar Ataxia 17 (SCAR17) is a very rare, inherited brain condition that mainly affects the cerebellum—the part that controls balance, movement coordination, and speech....
SCAR16 – Spinocerebellar Ataxia Autosomal Recessive Type 16 is a rare, inherited brain disorder. It mainly damages the cerebellum, the part of the brain that controls...
Autosomal recessive cerebellar ataxia caused by STIP1 homology and U-box containing protein-1 (STUB1/CHIP) deficiency is a genetic form of cerebellar ataxia. “Cerebellar ataxia” means slow, clumsy,...
Autosomal Recessive Cerebellar Ataxia Caused by Mutations in STUB1 (SCAR16) is a rare, inherited brain disease. It mainly harms the cerebellum, the part of the brain...
Autosomal recessive spinocerebellar ataxia 16 (SCAR16) is a rare, inherited brain disorder that mainly damages the cerebellum, the balance and coordination center. People slowly develop poor...
Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to rubcn (run and cysteine rich domain containing beclin 1 interacting protein) deficiency is a very rare, inherited brain...
