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Article

Brothers with constrictive pericarditis - A novel mutation in a rare disease.

Indian heart journal - 1 Sept 2016

Patil Devendra V, Phadke Milind S, Pahwa Jivtesh S, Dalal Ashwin B

Abstract excerpt

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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Source

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Identifiers

PMID: 27751317
DOI: 10.1016/j.ihj.2016.03.020
PMCID: PMC5067734

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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