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Results 1 - 10 of 13 for Paraparesis
  1. Troyer syndrome 
    ... of hereditary spastic paraplegia, also called hereditary spastic paraparesis. Hereditary spastic paraplegias are a group of genetic ... 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
  2. Spastic paraplegia type 15 
    ... SPASTIZIN: a close link between complicated hereditary spastic paraparesis and autophagy. Autophagy. 2014 Feb;10(2):374- ... 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
  3. Fatty acid hydroxylase-associated neurodegeneration 
    ... symptoms of the condition. Dysmyelinating leukodystrophy and spastic paraparesis FAHN Spastic paraplegia 35 Genetic Testing Registry: Hereditary ... hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia. Am J Hum Genet. 2008 Nov; ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  4. L1 syndrome 
    L1 syndrome describes a group of conditions that primarily affect the nervous system and occur almost exclusively in males. These conditions vary in severity ...
    https://medlineplus.gov/genetics/condition/l1-syndrome - Genetics
  5. ZFYVE26 gene 
    ... SPASTIZIN: a close link between complicated hereditary spastic paraparesis and autophagy. Autophagy. 2014 Feb;10(2):374- ... autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15. Brain. 2013 Oct;136(Pt 10): ...
    https://medlineplus.gov/genetics/gene/zfyve26 - Genetics
  6. Transcobalamin deficiency 
    ... experience progressive stiffness and weakness in their legs (paraparesis), muscle twitches (myoclonus), or intellectual disability.People with ...
    https://medlineplus.gov/genetics/condition/transcobalamin-deficiency - Genetics
  7. Lateral meningocele syndrome 
    ... paresthesias), progressive stiffness and weakness in the legs (paraparesis), and back pain can also occur. Delayed development ...
    https://medlineplus.gov/.../condition/lateral-meningocele-syndrome - Genetics
  8. X-linked adrenoleukodystrophy 
    ... develop progressive stiffness and weakness in their legs (paraparesis), experience urinary and genital tract disorders, and often ...
    https://medlineplus.gov/.../condition/x-linked-adrenoleukodystrophy - Genetics
  9. SPART gene 
    ... of hereditary spastic paraplegia (also called hereditary spastic paraparesis), a group of conditions that cause progressive stiffness ( ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
  10. TECPR2 gene 
    ... reveals a role for autophagy in hereditary spastic paraparesis. Am J Hum Genet. 2012 Dec 7;91( ...
    https://medlineplus.gov/genetics/gene/tecpr2 - Genetics
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