spinocerebellar degeneration

spinocerebellar degeneration

Friedreich's ataxia, see there.
References in periodicals archive ?
Furthermore, symmetric signal abnormalities of bilateral MCPs might also be apparent in other clinical conditions including Wilson disease, hepatic encephalopathy, extrapontine myelinolysis, acute disseminated encephalomyelitis, leukodystrophy, olivopontocerebellar atrophy, spinocerebellar degeneration, toluene abuse, adrenoleukodystrophy, alcoholic liver disease, hypoglycemic coma, and progressive multifocal leukoencephalopathy.[6],[7],[9],[17] Although these lesions are rare, clinicians still need to carefully identify them using clinical and laboratory investigations combined with imaging findings to prevent misdiagnosis.
Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration. Handb Clin Neurol.
She had been left paralysed from the neck down, unable to move her arms and legs due to a condition called spinocerebellar degeneration.
She had been left paralysed from the neck down, unable to move her arms and legs due to a condition called spinocerebellar degeneration. Two weeks after the operation, the prosthesis was connected and the woman embarked on 14 weeks of training -- but on only the second day, she was able to move the limb through mind power.
Jan suffers from spinocerebellar degeneration -a genetic disease - that has left her paralyzed from the neck down.
Friedreich's Ataxia, a spinocerebellar degeneration, is an inherited disease that causes progressive damage to the nervous system, resulting in muscle weakness, speech problems and heart disease.

Full browser ?