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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-...
Autores principales: | Xie, Peng, Huang, Jian-Min, Li, Huan-Li, Huang, Xiao-Jie, Wei, Ling-Ge |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
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 |
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