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Research Highlights

Huge French study of SPG4 HSP

New findings made

30-40% genetic diagnosis gap in HSPs

Need to look elsewhere for full picture of HSP genetics

Neurons more complex than thought

Prompts new view of how they function

Conventional view of SPG4 cause challenged

Additional mechanism suggested

New genetic type of HSP discovered

Associated with joint deformities in the feet and hands

Spinal cord changes in pure HSP

Matches with leg muscles affected

Damage in SPG4 extends to nerves of the feet

Measured by lack of sweating response

Spatial relationships different in SPG4 HSP brain

Size of difference related to clinical disability

New HSP genotypes and phenotypes

Research from China, Japan, Denmark, Czech Republic, Italy, Canada, Saudi Arabia, the UK and Portugal

Overview of the HSPs

Call for new classification

Posts pagination

Newer posts Page 1 … Page 15 … Page 45 Older posts

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.

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

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