New gene-disease associations found
Research Highlights
The science of patient input
Integrating patient needs and priorities
New Findings on SPG11 HSP mechanism
Potential treatment target identified
Late-onset spastic paraplegia type 10 (SPG10)
First-time discovered in an Asian family
REEP1 (SPG31) found with recessive inheritance
Previously associated only with dominant form
New HSP genetic findings
From Japan, Poland, England, China, Hungary, Morocco, Canada, Italy and the USA
Developing a ‘natural history’ of HSP
Large German study lays the foundation
Atlastin (SPG 3A) investigated
Questions raised about regulation and role
SPG 8 HSP loss-of-function theory questioned
Implications for alternative gain-of-function hypothesis
Brain shrinkage found in SPG 2 HSP
Changes also in the myelin sheath around axons
