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Results 1 - 10 of 23 for Spastic paraplegia 15
  1. Spastic paraplegia type 15 
    ... and symptoms of the condition. Autosomal recessive spastic paraplegia 15 Kjellin syndrome Spastic paraplegia and retinal degeneration SPG15 ... Hereditary spastic paraplegia Genetic Testing Registry: Hereditary spastic paraplegia 15 Autosomal recessive spastic paraplegia type 15 Hereditary spastic ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-15 - Genetics
  2. ZFYVE26 gene 
    ... ZFYVE26 gene have been found to cause spastic paraplegia type 15. This condition is characterized by progressive movement problems, ... responsible for many of the features of spastic paraplegia type 15.It is unclear whether a lack of spastizin ...
    https://medlineplus.gov/genetics/gene/zfyve26 - Genetics
  3. Neuromuscular Disorders (National Library of Medicine)  
    Neuromuscular disorders affect your neuromuscular system. They can cause problems with: The nerves that control your muscles Your muscles Communication between your ...
    https://medlineplus.gov/neuromusculardisorders.html - Health Topics
  4. Peripheral Nerve Disorders (National Library of Medicine)  
    What are peripheral nerves? Nerves are like wires that carry messages back and forth between your brain and your body. Your peripheral nerves branch off ...
    https://medlineplus.gov/peripheralnervedisorders.html - Health Topics
  5. SPG11 gene 
    ... common in familial cases of complicated hereditary spastic paraplegia. Neurology. 2008 Apr 15;70(16 Pt 2):1384-9. doi: 10. ... heterogeneity and genotype-phenotype correlations in hereditary spastic ... (SPG11). Eur J Neurol. 2008 Oct;15(10):1065-70. doi: 10.1111/j.1468- ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  6. Spastic paraplegia type 11 
    ... common in familial cases of complicated hereditary spastic paraplegia. Neurology. 2008 Apr 15;70(16 Pt 2):1384-9. doi: 10. ... heterogeneity and genotype-phenotype correlations in hereditary spastic ... (SPG11). Eur J Neurol. 2008 Oct;15(10):1065-70. doi: 10.1111/j.1468- ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-11 - Genetics
  7. Spastic paraplegia type 3A 
    ... 2 to 9 per 100,000 individuals. Spastic paraplegia type 3A accounts for 10 to 15 percent of all autosomal dominant hereditary spastic paraplegia cases. Mutations in the ATL1 gene cause spastic ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-3a - Genetics
  8. Spastic paraplegia type 8 
    ... M. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin. Am J Med Genet. 2000 May 15;92(2):122-7. doi: 10.1002/(sici) ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-8 - Genetics
  9. WASHC5 gene 
    ... M. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin. Am J Med Genet. 2000 May 15;92(2):122-7. doi: 10.1002/(sici) ...
    https://medlineplus.gov/genetics/gene/washc5 - Genetics
  10. Infantile-onset ascending hereditary spastic paralysis 
    ... J, Bohlega S. Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T. Gene. 2014 Feb 15;536(1):217-20. doi: 10.1016/j. ...
    https://medlineplus.gov/...et-ascending-hereditary-spastic-paralysis - Genetics
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