Bone Structural Characteristics and Response to Bisphosphonate Treatment in Children With Hajdu-Cheney Syndrome

CONTEXT: Hajdu-Cheney syndrome (HJCYS) is a rare, multisystem bone disease caused by heterozygous mutations in the NOTCH2 gene. Histomorphometric and bone ultrastructural analyses in children have not been reported and sparse evidence exists on response to bisphosphonate (BP) therapy. OBJECTIVE: To...

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Detalhes bibliográficos
Publicado no:J Clin Endocrinol Metab
Main Authors: Sakka, Sophia, Gafni, Rachel I., Davies, Justin H., Clarke, Bart, Tebben, Peter, Samuels, Mark, Saraff, Vrinda, Klaushofer, Klaus, Fratzl-Zelman, Nadja, Roschger, Paul, Rauch, Frank, Högler, Wolfgang
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2017
Assuntos:
Clinical Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5673271/
https://ncbi.nlm.nih.gov/pubmed/28938420
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2017-01102
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