Literature DB >> 15691357

Cardiac involvement in Emery-Dreifuss muscular dystrophy.

R Wessely1, S Seidl, A Schömig.   

Abstract

Emery-Dreifuss muscular dystrophy (EDMD) is a common form of muscular dystrophy frequently involving cardiac muscle, thus leading to dilated cardiomyopathy. Clinical outcome and prognosis is frequently determined by the involvement of the cardiac conduction system causing symptomatic bradyarrhythmias, as well as tachyarrhythmias and, if untreated, frequent sudden cardiac death. Typical features of the cardiac involvement of EDMD are presented, caused by a novel missense mutation in the splice receptor sequence of intron 6 of the LMNA gene on chromosome 1, encoding for the lamin A/C gene, consistent with the autosomal dominant form of EDMD.

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Year:  2005        PMID: 15691357     DOI: 10.1111/j.1399-0004.2004.00395.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  4 in total

1.  Attenuated hypertrophic response to pressure overload in a lamin A/C haploinsufficiency mouse.

Authors:  Mihaela Cupesi; Jun Yoshioka; Joseph Gannon; Anastacia Kudinova; Colin L Stewart; Jan Lammerding
Journal:  J Mol Cell Cardiol       Date:  2009-11-12       Impact factor: 5.000

2.  Torn apart: membrane rupture in muscular dystrophies and associated cardiomyopathies.

Authors:  Jan Lammerding; Richard T Lee
Journal:  J Clin Invest       Date:  2007-07       Impact factor: 14.808

Review 3.  Heart Disease in Disorders of Muscle, Neuromuscular Transmission, and the Nerves.

Authors:  Josef Finsterer; Claudia Stöllberger
Journal:  Korean Circ J       Date:  2016-03-21       Impact factor: 3.243

Review 4.  Management of cardiac involvement in muscular dystrophies: paediatric versus adult forms.

Authors:  Alberto Palladino; Paola D'Ambrosio; Andrea Antonio Papa; Roberta Petillo; Chiara Orsini; Marianna Scutifero; Gerardo Nigro; Luisa Politano
Journal:  Acta Myol       Date:  2016-12
  4 in total

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