merylg
Senior Member
- Messages
- 841
- Location
- Sydney, NSW, Australia
The cause of this has been found to be a mutation in the High Temperature Requirement-1 (HTRA1) gene. In the aberrant process, mutant HTRA1s have been shown to lose their protease activity leading to an increase in TGF-Beta family signalling.
TGF-Beta family signalling defects are associated with scoliosis & alopecia.
TGF-Beta family signalling defects are also associated with Marfan's/Loey Dietz Syndrome.
http://www.ncbi.nlm.nih.gov/pubmed/22277429
Angiotensin 1 Receptor Antagonist...a potential therapeutic...(already in use I believe)
Wondering how many with ME/CFS have a family history of vascular dementia? This could be part of the picture.
http://www.ncbi.nlm.nih.gov/pubmed/21301034
Hmmm...also thought to be associated with degenerative disc disease...
TGF-Beta family signalling defects are associated with scoliosis & alopecia.
TGF-Beta family signalling defects are also associated with Marfan's/Loey Dietz Syndrome.
http://www.ncbi.nlm.nih.gov/pubmed/22277429
Angiotensin 1 Receptor Antagonist...a potential therapeutic...(already in use I believe)
Wondering how many with ME/CFS have a family history of vascular dementia? This could be part of the picture.
http://www.ncbi.nlm.nih.gov/pubmed/21301034
Hmmm...also thought to be associated with degenerative disc disease...