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Results 1 - 10 of 12 for Progressive spastic paraparesis
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  1. HTLV-1-Associated Myelopathy (HAM)/Tropical Spastic Paraparesis (TSP) From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    HTLV-1-associated myelopathy (HAM)/tropical spastic paraparesis (TSP), or HAM/TSP, is a chronic and progressive disease of the nervous system that affects adults living in equatorial areas of the world.
    https://www.ninds.nih.gov/...thy-hamtropical-spastic-paraparesis-tsp - External Health Links
  2. SPART gene 
    ... type of hereditary spastic paraplegia (also called hereditary spastic paraparesis), a group of conditions that cause progressive stiffness (spasticity) and weakness of the leg muscles. ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
  3. Troyer syndrome 
    ... are a group of genetic disorders characterized by progressive stiffness (spasticity) and weakness of the leg muscles. The degree of leg weakness in people with hereditary spastic paraplegia can vary. Paraparesis is the term used to describe leg weakness, ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  4. Hereditary Spastic Paraplegia From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Peripheral Nerve Disorders/Specifics ... Peripheral Nerve Disorders ... Paralysis/Specifics ... Paralysis ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Leg ...
    https://www.ninds.nih.gov/.../hereditary-spastic-paraplegia - External Health Links
  5. Fatty acid hydroxylase-associated neurodegeneration 
    ... and symptoms of the condition. Dysmyelinating leukodystrophy and spastic paraparesis FAHN Spastic paraplegia 35 Genetic Testing Registry: Hereditary ... 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia. Am J Hum Genet. 2008 Nov; ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  6. Spastic paraplegia type 15 
    ... ZFYVE26/SPASTIZIN: a close link between complicated hereditary spastic paraparesis and autophagy. Autophagy. 2014 Feb;10(2):374- ... Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15. Brain. 2013 Oct;136(Pt 10): ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-15 - Genetics
  7. L1 syndrome 
    ... syndrome may have mild enlargement of the ventricles.Spastic paraplegia type 1 is characterized by progressive muscle stiffness (spasticity) and the development of paralysis ...
    https://medlineplus.gov/genetics/condition/l1-syndrome - Genetics
  8. ZFYVE26 gene 
    ... ZFYVE26/SPASTIZIN: a close link between complicated hereditary spastic paraparesis and autophagy. Autophagy. 2014 Feb;10(2):374- ... Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15. Brain. 2013 Oct;136(Pt 10): ...
    https://medlineplus.gov/genetics/gene/zfyve26 - Genetics
  9. Spastic paraplegia type 49 
    ... TECPR2 reveals a role for autophagy in hereditary spastic paraparesis. Am J Hum Genet. 2012 Dec 7;91( ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-49 - Genetics
  10. FA2H gene 
    ... 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia. Am J Hum Genet. 2008 Nov; ...
    https://medlineplus.gov/genetics/gene/fa2h - Genetics
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