Camurati–Engelmann disease-a rare cause of tetany identified on bone scintigraphy: A case report

RATIONALE: Camurati–Engelmann disease (i.e., progressive diaphyseal dysplasia) is an extremely rare autosomal dominant bone disorder. The most common clinical manifestations were chronic skeletal pain, waddling gait, muscular weakness. PATIENT CONCERNS: We described that a 27-year-old male with a 1-...

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Detalles Bibliográficos
Autores principales: Xie, Peng, Huang, Jian-Min, Li, Huan-Li, Huang, Xiao-Jie, Wei, Ling-Ge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
6800
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502140/
https://www.ncbi.nlm.nih.gov/pubmed/28682867
http://dx.doi.org/10.1097/MD.0000000000007141

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502140/
https://www.ncbi.nlm.nih.gov/pubmed/28682867
http://dx.doi.org/10.1097/MD.0000000000007141

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