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Research Highlights

HSP types and patterns similar globally

Large study in China confirms previous findings

New findings on SPG54 HSP

Mitochondria now implicated

New HSP genotypes and phenotypes

Research from China, Japan, Germany, Turkey and Australia

Mitochondrial impairment studied in SPG15 & 48 HSP

Function restored with treatment in lab experiments

SPG10 HSP gene now linked with Motor Neurone Disease

Previously linked to Charcot Marie Tooth

New HSP gene ACO2 discovered

Associated with recessive complicated HSP

Mechanism of AP-4 related HSPs investigated

AP-4 deficiency underlies four types of HSP

SPAST mutation affects adjacent gene

Combined effect causes complicated HSP

EPT1 mutation causes complicated HSP

Affects myelin sheath that covers nerves

Parkinsonism found in SPG7 HSP

Responsive to levodopa treatment

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Newer posts Page 1 … Page 17 … 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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