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Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by WWOX mutation is a rare, inherited brain and nerve disorder caused by harmful changes (variants) in a single...
Autosomal recessive spinocerebellar ataxia 12 (SCAR12) is a very rare, inherited brain disorder. Children with SCAR12 usually start having generalized seizures in infancy, followed by delayed motor...
SYT14-related autosomal recessive syndromic cerebellar ataxia is a rare inherited brain disorder. It mainly affects the cerebellum, the part of the brain that controls balance, coordination,...
Autosomal recessive syndromic cerebellar ataxia caused by mutation in SYT14 (SCAR11) is a rare, inherited brain disorder that mainly affects the cerebellum, the part of the...
Autosomal recessive cerebellar ataxia–psychomotor delay syndrome is a rare, inherited brain disorder. “Autosomal recessive” means a child gets one faulty gene from each parent. Parents are...
Autosomal Recessive Spinocerebellar Ataxia 11 (SCAR11) is a very rare genetic brain disorder that mainly damages the cerebellum, the part of the brain that controls balance,...
Spinocerebellar ataxia (SCA) is a group of rare, inherited brain disorders. In SCA, parts of the brain that control balance and coordination—especially the cerebellum—slowly get damaged....
Autosomal Recessive Cerebellar Ataxia Caused by ANO10 Mutation is a rare, inherited brain disorder in which both copies of a person’s ANO10 gene are changed (mutated)....
ANO10 autosomal recessive cerebellar ataxia is a rare, inherited brain disorder. It mainly affects the cerebellum, the part of the brain that controls balance, walking, and...
Autosomal recessive spinocerebellar ataxia 10 (SCAR10) is a rare, inherited brain disorder that mainly affects the cerebellum—the part that coordinates balance, speech, and eye movements. It...
CAPN1 autosomal recessive complex spastic paraplegia is a rare inherited nerve disorder. It mainly damages the long movement pathways that run from the brain to the...
Autosomal recessive complex spastic paraplegia caused by mutations in CAPN1 is a rare inherited nerve disorder. It mainly makes the legs stiff and tight (spastic), so...
