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...

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Detalles Bibliográficos
Autores principales: Patil, Devendra V., Phadke, Milind S., Pahwa, Jivtesh S., Dalal, Ashwin B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Images in Cardiology
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

Internet

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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