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Autosomal recessive cerebellar ataxia with late-onset spasticity (often shortened to ARCA-LOS) is a rare inherited brain and nerve disorder. “Cerebellar ataxia” means the balance and coordination...
Autosomal recessive cerebellar ataxia–pyramidal signs–nystagmus–oculomotor apraxia syndrome (ARCA-PS-N-OMA) is a very rare, inherited brain disorder. “Autosomal recessive” means a child gets one nonworking gene copy from...
Autosomal recessive neuromyotonia and axonal neuropathy is a rare, inherited nerve disease. It starts in childhood or the teen years. It damages the axons (the long...
Autosomal recessive axonal neuropathy with neuromyotonia is a rare, inherited nerve disease. It starts when both copies of a person’s HINT1 gene carry harmful changes (mutations)....
Autosomal recessive axonal Charcot-Marie-Tooth disease due to a copper-metabolism defect is a very rare inherited nerve disease. It mainly damages the long “wires” (axons) of the...
Spinocerebellar ataxia, autosomal recessive type 8 (SCAR8) is a rare, inherited brain disorder. It mainly affects the cerebellum, the part of the brain that controls balance...
Autosomal recessive cerebellar ataxia type 1 (ARCA1) is a rare, inherited brain condition that mainly affects the cerebellum, the part of the brain that controls balance,...
Autosomal recessive ataxia, Beauce type is a rare, inherited brain condition that mainly affects the cerebellum, the part of the brain that controls balance and coordination....
Autosomal recessive spinocerebellar ataxia type 9 (SCAR9) is a rare inherited brain disorder that mainly affects the cerebellum, the part of the brain that organizes balance...
Autosomal recessive ataxia due to CoQ10 deficiency is a rare, inherited brain and muscle energy problem. Your body makes CoQ10 to help mitochondria (the cell’s “power...
Autosomal recessive cerebellar ataxia type 2 (ARCA2) is a rare, inherited brain disorder. It happens when both copies of a gene called COQ8A (also known as...
Autosomal recessive ataxia due to ubiquinone deficiency is a genetic, inherited condition in which the body cannot make enough coenzyme Q10 (CoQ10, also called ubiquinone). CoQ10...
