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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-...
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| Publicat a: | Medicine (Baltimore) |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer Health
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5502140/ https://ncbi.nlm.nih.gov/pubmed/28682867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000007141 |
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