Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 20 for Spastic ataxia
  1. Autosomal recessive spastic ataxia of Charlevoix-Saguenay 
    Autosomal recessive spastic ataxia of Charlevoix-Saguenay, more commonly known as ARSACS, is a condition affecting muscle movement. People with ARSACS typically ...
    https://medlineplus.gov/...ive-spastic-ataxia-of-charlevoix-saguenay - Genetics
  2. Andermann syndrome 
    ... N, Bouchard JP, Brais B, Rouleau GA. Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian population. ...
    https://medlineplus.gov/genetics/condition/andermann-syndrome - Genetics
  3. GLUT1 deficiency syndrome 
    ... as stiffness caused by abnormal tensing of the muscles (spasticity), difficulty in coordinating movements (ataxia), and speech difficulties (dysarthria). Some experience episodes of ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
  4. Spastic paraplegia type 7 
    ... 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- ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
  5. Spastic paraplegia type 5A 
    ... EFNS. EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. Eur J Neurol. 2010 Feb;17(2): ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-5a - Genetics
  6. Free sialic acid storage disorder 
    ... and symptoms include problems with movement and balance (ataxia); abnormal tensing of the muscles (spasticity); and involuntary slow, writhing movements of the limbs ( ...
    https://medlineplus.gov/.../free-sialic-acid-storage-disorder - Genetics
  7. Transthyretin amyloidosis 
    ... fluid in the brain (hydrocephalus), difficulty coordinating movements (ataxia), muscle stiffness and weakness (spastic paralysis), seizures, and loss of intellectual function (dementia). ...
    https://medlineplus.gov/genetics/condition/transthyretin-amyloidosis - Genetics
  8. TUBB4A-related leukodystrophy 
    ... muscle stiffness and paralysis of the lower limbs (spastic paraplegia) that slowly worsen. In addition, these individuals may have mild hypomyelination and ataxia without the other movement or learning problems common ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  9. Troyer syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  10. Spastic paraplegia type 2 
    ... additional features. People with the complex form of spastic paraplegia type 2 have lower limb spasticity and can also experience problems with movement and balance (ataxia); involuntary movements of the eyes (nystagmus); mild intellectual ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-2 - Genetics
previous · 1 · 2 · next