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Hereditær spastisk paraparese HSP

Sist oppdatert: Sist revidert:
Sist revidert av:
  1. Shribman S, Reid E, Crosby AH, Houlden H, Warner TT. Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches. Lancet Neurol. 2019 Dec;18(12):1136-1146. PMID: 31377012. PubMed  
  2. Erichsen AK, Koht J, Stray-Pedersen A, Abdelnoor M, Tallaksen CM. Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study. Brain. 2009 Jun;132(Pt 6):1577-88. PMID: 19339254 PubMed  
  3. Ruano L, Melo C, Silva MC, Coutinho P. The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies. Neuroepidemiology. 2014;42(3):174-83. PMID: 24603320 PubMed  
  4. Tesson C, Koht J, Stevanin G. Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology.Hum Genet. 2015 Jun;134(6):511-38. PMID: 25758904 PubMed  
  5. de Souza PVS, de Rezende Pinto WBV, de Rezende Batistella GN, Bortholin T, Oliveira ASB. Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks.Cerebellum. 2017 Apr;16(2):525-551. PMID: 27271711 PubMed  
  6. Murala S, Nagarajan E, Bollu PC. Hereditary spastic paraplegia. Neurol Sci. 2021 Mar;42(3):883-894. doi: 10.1007/s10072-020-04981-7. Epub 2021 Jan 13. PMID: 33439395. PubMed  
  7. Marras C, Lang A, van de Warrenburg BP, Sue CM, Tabrizi SJ, Bertram L, Mercimek-Mahmutoglu S, Ebrahimi-Fakhari D, Warner TT, Durr A, Assmann B, Lohmann K, Kostic V, Klein C.Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force. Mov Disord. 2017 May;32(5):724-725. PMID: 28513081 PubMed  
  8. Boutry M, Morais S, Stevanin G. Update on the Genetics of Spastic Paraplegias.Curr Neurol Neurosci Rep. 2019 Feb 28;19(4):18. PMID: 30820684 PubMed  
  9. Parodi L, Fenu S, Barbier M, Banneau G, Duyckaerts C, Tezenas du Montcel S, Monin ML, Ait Said S, Guegan J, Tallaksen CME, Sablonniere B, Brice A, Stevanin G, Depienne C, Durr A; SPATAX network . Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex. Brain. 2018 Dec 1;141(12):3331-3342. PMID: 30476002 PubMed  
  10. Erfanian Omidvar M, Torkamandi S, Rezaei S, Alipoor B, Omrani MD, Darvish H, Ghaedi H. Genotype-phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients. J Neurol. 2019 Nov 19. PMID: 31745725. PubMed  
  • Siri Lynne Rydning, spesialist i nevrologi
  • Jeanette Koht, spesialist i nevrologi, PhD
  • Chantal Tallaksen, spesialist i nevrologi, professor dr med
  • Unn Ljøstad, spesialist i nevrologi, professor PhD
  • Åse Mygland, spesialist i nevrologi, professor dr med