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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Spastic paraplegia 23


Other Names for this Disease
  • Autosomal recessive spastic paraplegia type 23
  • Lison syndrome
  • Spastic paraplegia and pigmentary abnormalities
  • Spastic paraplegia vitiligo premature graying and characteristic facies
  • SPG 23
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Treatment


Clinical Trials & Research for this Disease

  • The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.