Literature DB >> 15724423

[Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation].

J E Forissier1, G Bonne, C Bouchier, L Duboscq-Bidot, P Richard, S Briault, C Moraine, O Dubourg, K Schwartz, M Komajda.   

Abstract

UNLABELLED: Mutations in LMNA gene encoding two ubiquitously expressed nuclear proteins, lamins A and C, give rise to up to 7 different pathologies affecting specific tissues. Three of these disorders affect cardiac and/or skeletal muscles with atrio-ventricular conduction disturbances, dilated cardiomyopathy and sudden cardiac death as common features.
RESULTS: A new LMNA mutation (1621C>T, R541C) was found in two members of a French family with a history of ventricular rhythm disturbances and an uncommon form of systolic left ventricle dysfunction. The two patients: the proband and his daughter, were affected and exhibited an atypical form of dilated cardiomyopathy with an unexplained left ventricle aneurysm revealed by ventricular rhythm disturbances without atrio-ventricular block.
CONCLUSION: This finding reinforces the highly variable phenotypic expression of LMNA mutation and emphasizes the fact that LMNA mutations can be associated with different cardiac phenotypes.

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Year:  2005        PMID: 15724423

Source DB:  PubMed          Journal:  Arch Mal Coeur Vaiss        ISSN: 0003-9683


  2 in total

Review 1.  Genetics of inherited cardiomyopathies in Africa.

Authors:  Gasnat Shaboodien; Timothy F Spracklen; Stephen Kamuli; Polycarp Ndibangwi; Carla Van Niekerk; Ntobeko A B Ntusi
Journal:  Cardiovasc Diagn Ther       Date:  2020-04

2.  Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation.

Authors:  Najlae Adadi; Fatima Zohra Radi; Najim Lahrouchi; Loubna Hara; Ilham Ratbi; Siham Chafai Elalaoui; Marielle Alders; Jamila Zarzur; Connie Bezzina; Abdelaziz Sefiani
Journal:  Anatol J Cardiol       Date:  2018-07       Impact factor: 1.596

  2 in total

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