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Brothers with constrictive pericarditis - A novel mutation in a rare disease
Devendra V Patil1, Milind S Phadke2, Jivtesh S Pahwa1
1Resident, KEMH - Seth GS medical College and KEM Hospital, Parel, Mumbai, India.
Abstract:
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 CACP syndrome and also revealed a rare mutation in the causative gene.
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