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Spastic ataxia 3
- ... Topaloglu H. Private SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) families from Turkey. Neurogenetics. 2004 Sep;5(3):165-70. doi: 10.1007/s10048-004-0179- ...
- ... usually becomes evident by about the age of 3. It most often appears as stiffness, ... (ataxia). Occasionally, high-protein meals or stress caused by ...
- ... 1252-7. doi: 10.1007/s00415-009-5109-3. Epub 2009 Apr 12. Citation on PubMed ... diagnosis of ataxias and spastic paraplegias. Eur J Neurol. 2010 Feb;17(2): ...
- ... 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; ... homeostasis and neurodegeneration. Cell Res. 2018 Mar;28(3):296-306. doi: ... a common cause of undiagnosed ataxia. Neurology. 2015 May 5;84(18):1911. doi: ...
- ... 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). ...
- ... involve the legs and the bladder. Complex hereditary spastic paraplegias may include additional signs and symptoms such as intellectual disabilities, problems with coordination and balance (ataxia), and damage to the nerves that connect the ...
- ... III Autosomal recessive OPA3 Autosomal recessive optic atrophy 3 Costeff optic atrophy syndrome Infantile optic atrophy with chorea and spastic paraplegia Iraqi Jewish optic atrophy plus MGA, type ...