Skip to content
HSP Logo Hereditary Spastic Paraplegia - Taking steps to towards a cure
  • Home
  • The Foundation
    • Foundation Committee 2021/22
    • Annual Reports
  • About HSP
    • What is HSP?
    • Understanding the HSP Mechanism
    • Research Background
    • Living with HSP – Management & Treatment Background
  • Genes & HSP
    • Genetic Testing Services
    • Gene Testing Q & A
  • HSP Research
  • Resources
    • Applying for the NDIS
    • Community Recommended Practitioner Listings
    • Recommend your health professional here
  • Get Involved
    • Join the HSP community
  • Contact Us
  • Current Appeal
    • Past Appeals
  • Give
    • Giving
    • Leave a Bequest
    • Fundraising

SPG10–related HSP studied

SPG10 patients have pure HSP

J Neurol Neurosurg Psychiatry. 2008 Feb 1

   

   

Posted May 2008 in Research Highlights

Related posts

Spastin levels found to be important
Link between HSP & Charcot-Marie-Tooth disease
SPG10 HSP and CMT type 2 strongly linked
Medical research in the digital age
Brain changes in SPG4 HSP measured

HSP Research Foundation

Welcome to the HSP Research Foundation - created in 2005 to find a cure for Hereditary Spastic Paraplegia - an inherited, degenerative disease affecting mainly the legs, causing muscle weakness, spasticity and severely impairing walking. Read more »

Information on this website and resources to which we have links are general knowledge about HSP. We are not medical professionals, nor do we offer medical advice. Always consult your own medical professionals regarding your particular circumstances.

Registered charity

The HSP Research Foundation Incorporated ABN 46648875912 is an Income Tax Exempt Charity endorsed by the ATO as a Deductible Gift Recipient organisation.

© Copyright 2006 - 2021 HSP Research Foundation | Privacy Policy