Hutchinson-Gilford Progeria Is a Skeletal Dysplasia

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare segmental premature aging disorder that affects bone and body composition, among other tissues. We sought to determine if bone density and structural geometry are altered in children with HGPS, and whether relationships exist among these paramete...

Full description

Saved in:
Bibliographic Details
Published in:J Bone Miner Res
Main Authors: Gordon, Catherine M., Gordon, Leslie B., Snyder, Brian D., Nazarian, Ara, Quinn, Nicolle, Huh, Susanna, Giobbie-Hurder, Anita, Neuberg, Donna, Cleveland, Robert, Kleinman, Monica, Miller, David T., Kieran, Mark W.
Format: Artigo
Language:Inglês
Published: 2011
Subjects:
Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5650062/
https://ncbi.nlm.nih.gov/pubmed/21445982
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.392
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items