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Camurati-Engelmann Disease with Good Treatment Response to Losartan
Camurati–Engelmann disease (CED) or progressive diaphyseal dysplasia is a rare autosomal dominant inherited condition which belongs to the group of craniotubular hyperostosis. A 24-year-old man presented with insidious onset, progressive pain over both legs, and forearms for 3 years. He was born as...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593949/ https://www.ncbi.nlm.nih.gov/pubmed/31293304 http://dx.doi.org/10.4103/ijnm.IJNM_44_19 |