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Brothers with constrictive pericarditis – A novel mutation in a rare disease
Familial constrictive pericarditis is extremely rare. We report a case of two brothers both suffering constrictive pericarditis along with having multiple painless joint deformities. Genetic workup confirmed the clinical diagnosis of camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome C...
Autores principales: | Patil, Devendra V., Phadke, Milind S., Pahwa, Jivtesh S., Dalal, Ashwin B. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067734/ https://www.ncbi.nlm.nih.gov/pubmed/27751317 http://dx.doi.org/10.1016/j.ihj.2016.03.020 |
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