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Spastic ataxia
- Autosomal recessive spastic ataxia of Charlevoix-Saguenay, more commonly known as ARSACS, is a condition affecting muscle movement. People with ARSACS typically ...
- ... gene have been found to cause autosomal recessive spastic ataxia of Charlevoix-Saguenay, commonly called ARSACS. ARSACS is ... Condition ARSACS DNAJC29 KIAA0730 PPP1R138 SACS_HUMAN sacsin spastic ataxia of Charlevoix-Saguenay (sacsin) SPAX6 Tests of SACS ...
- ... Hair color (light or dark hair) Autosomal recessive spastic ataxia of Charlevoix-Saguenay , also called ARSACS Andermann syndrome , ...
- ... are a frequent cause of sporadic and recessive spastic ataxia. Brain. 2017 Jun 1;140(6):1561-1578. ...
- ... N, Bouchard JP, Brais B, Rouleau GA. Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian population. ...
- ... as stiffness caused by abnormal tensing of the muscles (spasticity), difficulty in coordinating movements (ataxia), and speech difficulties (dysarthria). Some experience episodes of ...
- ... some muscle weakness. People with this form of spastic paraplegia can also have ataxia; a pattern of movement abnormalities known as parkinsonism; ... SPG7 mutations are a common cause of undiagnosed ataxia. Neurology. 2015 May ... mutations in hereditary spastic paraplegia. Brain. 2004 May;127(Pt 5):973- ...
- ... EFNS. EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. Eur J Neurol. 2010 Feb;17(2): ...
- ... and symptoms include problems with movement and balance (ataxia); abnormal tensing of the muscles (spasticity); and involuntary slow, writhing movements of the limbs ( ...
- ... fluid in the brain (hydrocephalus), difficulty coordinating movements (ataxia), muscle stiffness and weakness (spastic paralysis), seizures, and loss of intellectual function (dementia). ...
