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Research Highlights

SPG7 HSP discoveries

Wide spectrum of HSP forms

22 genes & 48 locations for HSP

How many more to find?

New gene interacts with Spastin

Implicated in cell structural abnormalities

HSP and its ‘cousin’ CMT

Comparing genetics and cell function

Assessing nerve abnormalities in HSP

New measurement method tested

Large study of SPG31

Both pure & complex HSP found

Questions raised about Botox

muscle loss and weakness with long term use

Large HSP survey in Japan

321 HSPers from 144 families registered

New HSP gene testing method

Sporadic HSP cases analysed

Link between reflexes and spasticity questioned

Over-active reflexes and calf muscle spasticity

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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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