Literature DB >> 18815187

Complete atrioventricular block in Duchenne muscular dystrophy.

A Fayssoil1, D Orlikowski, O Nardi, D Annane.   

Abstract

Duchenne muscular dystrophy (DMD) is an inherited myogenic disorder due to mutations in the dystrophin gene on chromosome Xp21.1. It is characterized by progressive muscle wasting and weakness of variable distribution and severity. Heart is involved leading to heart failure. Conduction abnormalities are unusual. We report a case of complete atrio-ventricular block in a DMD patient.

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Year:  2008        PMID： 18815187     DOI： 10.1093/europace/eun264

Source DB:  PubMed          Journal:  Europace        ISSN： 1099-5129            Impact factor:   5.214


  6 in total

1.  Complete AV block and cardiac syncope in a patient with Duchenne muscular dystrophy.

Authors:  Refik Emre Altekin; Atakan Yanikoglu; Mustafa Ucar; Cengiz Ermis
Journal:  J Cardiol Cases       Date:  2011-02-16

Review 2.  Treatment of dystrophin cardiomyopathies.

Authors:  Josef Finsterer; Linda Cripe
Journal:  Nat Rev Cardiol       Date:  2014-01-14       Impact factor: 32.419

3.  Interventions for preventing and treating cardiac complications in Duchenne and Becker muscular dystrophy and X-linked dilated cardiomyopathy.

Authors:  John P Bourke; Teofila Bueser; Rosaline Quinlivan
Journal:  Cochrane Database Syst Rev       Date:  2018-10-16

Review 4.  Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy.

Authors:  Abdallah Fayssoil; Soumeth Abasse; Katy Silverston
Journal:  J Neuromuscul Dis       Date:  2017

Review 5.  Advances in Stem Cell Modeling of Dystrophin-Associated Disease: Implications for the Wider World of Dilated Cardiomyopathy.

Authors:  Josè Manuel Pioner; Alessandra Fornaro; Raffaele Coppini; Nicole Ceschia; Leonardo Sacconi; Maria Alice Donati; Silvia Favilli; Corrado Poggesi; Iacopo Olivotto; Cecilia Ferrantini
Journal:  Front Physiol       Date:  2020-05-12       Impact factor: 4.566

6.  Cardiac resynchronization therapy in a young patient with Duchenne muscular dystrophy.

Authors:  Tamami Kono; Akiyoshi Ogimoto; Kazuhisa Nishimura; Toshihiro Yorozuya; Takafumi Okura; Jitsuo Higaki
Journal:  Int Med Case Rep J       Date:  2015-08-21
  6 in total

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