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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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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.