26 top medical experts on Spastic paraplegia 23 across 6 countries and 1 U.S. states, including 2 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Spastic paraplegia 23: Autosomal recessive spastic paraplegia type 23 (SPG23) is a rare, complex type of hereditary spastic paraplegia that presents in childhood with progressive spastic paraplegia, associated with peripheral neuropathy, skin pigment abnormalities (i.e. vitiligo, hyperpigmentation, diffuse lentigines), premature graying of hair, and characteristic facies (i.e. thin with ''sharp'' features). The SPG23 phenotype has been mapped to a locus on chromosome 1q24-q32.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Social Networking Websites

  • RareConnect is an online social network for patients and families to connect with one another and share their experience living with a rare disease. The project is a joint collaboration between EURORDIS (European Rare Disease Organisation) and NORD (National Organization for Rare Disorders). Click on the link above to view the community for Hereditary spastic paraplegia.
  • Synonyms: Abdallat Davis Farrage syndrome,  Abdallat syndrome,  Lison syndrome,  Characteristic Facies Premature Graying Vitiligo Spastic Paraparesis,  Spastic Paraplegia With Pigmentary Abnormalities,  Spastic paraplegia and pigmentary abnormalities,  premature graying and characteristic facies vitiligo Spastic paraplegia


    •   

            

                        


      Computing Expert Listing ...