Find disease guides, symptoms, medicines, lab tests, and patient-friendly medical resources.
56,125 results found
You searched for “X” in All. RX Search found 56,125 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Autosomal recessive cerebellar ataxia–epilepsy–intellectual disability syndrome due to RUBCN deficiency is a very rare inherited brain disorder. It usually begins in early childhood. Children have problems...
Autosomal Recessive Spinocerebellar Ataxia 15 (SCAR15) is a very rare, inherited brain disorder. It mainly affects the cerebellum, the part of the brain that controls balance,...
SPTBN2 autosomal recessive cerebellar ataxia is a rare, inherited brain disorder that mainly affects the cerebellum—the part of the brain that controls balance, coordination, eye movements,...
Spectrin-associated autosomal recessive cerebellar ataxia type 1 (SPARCA1) is a rare, inherited brain disorder. “Autosomal recessive” means a child is affected when they receive one faulty...
Infantile-onset spinocerebellar ataxia is a genetic condition that appears after a period of normal early development. In early childhood, children begin to have unsteady movements, low...
Autosomal recessive cerebellar ataxia–cognitive defect syndrome is a group of rare genetic diseases. A child gets one faulty copy of a gene from each parent. Parents...
Autosomal recessive cerebellar ataxia caused by SPTBN2 mutations is a childhood-onset cerebellar ataxia caused by pathogenic variants in both copies of the SPTBN2 gene. SPTBN2 makes...
Ataxie Spinocérébelleuse à début infantile avec retard psychomoteur is most often called autosomal recessive spinocerebellar ataxia type 14 (SCAR14) and is caused by changes (variants) in...
Autosomal recessive spinocerebellar ataxia 14 (SCAR14) is a rare, inherited brain disorder. It mainly affects the cerebellum, which controls balance, movement, and eye control. Children usually...
WWOX autosomal recessive cerebellar ataxia–epilepsy–intellectual disability syndrome is a rare, inherited brain disorder that starts in infancy or early childhood. Because of a faulty gene called...
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX (WW domain-containing oxidoreductase) deficiency is a rare, inherited brain disorder that starts very early in...
Autosomal Recessive Cerebellar Ataxia–Epilepsy–Intellectual Disability Syndrome due to WWOX Deficiency is a rare, inherited brain disorder. A baby is born with two faulty copies of a...
