Extraskeletal Calcifications in Hutchinson-Gilford Progeria Syndrome

PURPOSE. Children with Hutchinson-Gilford progeria syndrome (HGPS), a rare premature aging disease, exhibit extraskeletal calcifications detected by radiographic analysis and on physical examination. The aim of this study was to describe the natural history and pathophysiology of these abnormal calc...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Bone
Päätekijät: Gordon, CM, Cleveland, RH, Baltrusaitis, K, Massaro, J, D’Agostino, RB, Liang, MG, Snyder, B, Walters, M, Li, X, Braddock, DT, Kleinman, ME, Kieran, MW, Gordon, LB.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2019
Aiheet:
Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6628204/
https://ncbi.nlm.nih.gov/pubmed/31077852
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2019.05.008
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