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Research Highlights

SPG 31 studied in mice

Impaired cell structure connected with symptoms

Spastin found to associate with lipid droplets

Further study may lead to therapies

Spastin role in central nervous system development

Important in the structure that houses the brainstem

Next Generation Sequencing diagnostics for HSPs

Germany leading in HSP gene testing

HSP gene testing advance in China

Success in detecting point mutations

Next generation gene testing

Helps identify non-SPG4 HSP

Sharing genetics knowledge

New software will aid progress

Calf muscle spasticity studied

Lengthening the muscle may help

Nerve conduction impairment in HSP studied

Signals to & from the brain are very different

The blood-brain barrier

Dr Karl explains

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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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