[feed] Atom [feed] RSS 1.0 [feed] RSS 2.0

Patil, D.V. and Phadke, M.S. and Pahwa, J.S. and Dalal, Ashwin (2016) Brothers with constrictive pericarditis – A novel mutation in a rare disease. Indian Heart Journal, 68 (S2). S284-S287. ISSN 0019-4832

[img] Text
Ind Heart J in press.pdf
Restricted to Repository staff only

Download (1312Kb) | Request a copy

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.

Item Type: Article
Additional Information: Open Access from the Publisher
Depositing User: Dr P Divakar
Date Deposited: 29 Apr 2016 04:04
Last Modified: 21 Oct 2016 06:53
URI: http://cdfd.sciencecentral.in/id/eprint/717

Actions (login required)

View Item View Item