AB030. Study of bone turnover markers and treatment monitoring in osteogenesis imperfecta

BACKGROUND: Osteogenesis imperfecta (OI), the most prevalent heritable disorders of bone, results from mutations involving several genes responsible for the synthesis or intracellular processing of type I collagen. Bisphosphonates are potent antiresorptive agents, decreasing the incidence of fractur...

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Dettagli Bibliografici
Pubblicato in:Ann Transl Med
Autori principali: Gouda, Amr, Temtamy, Samia, Ali, Ola, Nazim, Walaa, Aglan, Mona, Otaify, Ghada
Natura: Artigo
Lingua:Inglês
Pubblicazione: AME Publishing Company 2017
Soggetti:
Birth Defects, Dysmorphology, Skeletal Dysplasia, Craniofacial Anomalies
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5641747/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s030
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