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Results 1 - 10 of 22 for spastic
  1. SPART gene 
    ... syndrome. More About This Health Condition KIAA0610 SPARTIN spastic paraplegia 20 spastic paraplegia 20 (Troyer syndrome) spastic paraplegia 20, spartin ( ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
  2. SPG7 gene 
    ... the SPG7 gene have been found to cause spastic paraplegia type 7. This condition is characterized by ... leading to the major signs and symptoms of spastic paraplegia type 7. More About This Health Condition ...
    https://medlineplus.gov/genetics/gene/spg7 - Genetics
  3. SPG11 gene 
    ... the SPG11 gene have been found to cause spastic paraplegia type 11. Most of these mutations change ... spatacsin may cause the signs and symptoms of spastic paraplegia type 11 by interfering with the protein' ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  4. SACS gene 
    ... gene have been found to cause autosomal recessive spastic ataxia of Charlevoix-Saguenay, commonly called ARSACS. ARSACS ... that is characterized by abnormal tensing of the muscles (spasticity), problems with balance and coordination (cerebellar ataxia), and ...
    https://medlineplus.gov/genetics/gene/sacs - Genetics
  5. SPAST gene 
    ... the SPAST gene have been found to cause spastic paraplegia type 4. This condition is characterized by ... contribute to the major signs and symptoms of spastic paraplegia type 4.Mutation in the SPAST gene ...
    https://medlineplus.gov/genetics/gene/spast - Genetics
  6. FA2H gene 
    ... once classified as having a separate disorder called spastic paraplegia 35. People with mutations in this gene ... acid hydroxylase domain containing 1 FAXDC1 FLJ25287 SCS7 spastic paraplegia 35 (autosomal recessive) SPG35 Tests of FA2H ...
    https://medlineplus.gov/genetics/gene/fa2h - Genetics
  7. C19orf12 gene 
    ... are considered to have a condition called hereditary spastic paraplegia type 43. More About This Health Condition ... S, Blackstone C, Fischbeck KH, Burnett BG. Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics
  8. OPA3 gene 
    ... optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) Tests of OPA3 PubMed OUTER MITOCHONDRIAL MEMBRANE ...
    https://medlineplus.gov/genetics/gene/opa3 - Genetics
  9. ATL1 gene 
    ... the ATL1 gene have been found to cause spastic paraplegia type 3A. This condition is characterized by ... in childhood. Most of the mutations that cause spastic paraplegia type 3A change one protein building block ( ...
    https://medlineplus.gov/genetics/gene/atl1 - Genetics
  10. WASHC5 gene 
    ... the WASHC5 gene have been found to cause spastic paraplegia type 8. These mutations change single building ... muscle weakness, muscle stiffness, and other features of spastic paraplegia type 8. More About This Health Condition ...
    https://medlineplus.gov/genetics/gene/washc5 - Genetics
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