Literature DB >> 19078768

Epidermolysis bullosa simplex associated with muscular dystrophy and cardiac involvement.

Canan Celik1, Hilmi Uysal, Aylin Okcu Heper, Belgin Karaoglan.   

Abstract

We report a new clinical variant of epidermolysis bullosa simplex with muscular dystrophy (EBS-MD) that was associated with cardiac involvement. A 33-year-old patient had atrial fibrillation, pericardial effusion, and hypokinetic left ventricular cardiac walls. The muscle biopsy material revealed diffuse endomysial fibrosis and small atrophic muscle fibers with rounded contours. A positive desmin expression with abnormal localization in the subsarcolemmal groups was observed. We concluded that patients with EBS-MD should be investigated carefully when there are associated cardiac findings.

Entities:  

Year:  2005        PMID: 19078768     DOI: 10.1097/01.cnd.0000159779.32828.e7

Source DB:  PubMed          Journal:  J Clin Neuromuscul Dis        ISSN: 1522-0443


  6 in total

1.  Analysis of selected genes associated with cardiomyopathy by next-generation sequencing.

Authors:  Viktoria Szabadosova; Iveta Boronova; Peter Ferenc; Iveta Tothova; Jarmila Bernasovska; Michaela Zigova; Jan Kmec; Ivan Bernasovsky
Journal:  J Clin Lab Anal       Date:  2017-06-08       Impact factor: 2.352

2.  A Missense Variant in PLEC Increases Risk of Atrial Fibrillation.

Authors:  Rosa B Thorolfsdottir; Gardar Sveinbjornsson; Patrick Sulem; Anna Helgadottir; Solveig Gretarsdottir; Stefania Benonisdottir; Audur Magnusdottir; Olafur B Davidsson; Sridharan Rajamani; Dan M Roden; Dawood Darbar; Terje R Pedersen; Marc S Sabatine; Ingileif Jonsdottir; David O Arnar; Unnur Thorsteinsdottir; Daniel F Gudbjartsson; Hilma Holm; Kari Stefansson
Journal:  J Am Coll Cardiol       Date:  2017-10-24       Impact factor: 24.094

Review 3.  Myofibrillar myopathy in the genomic context.

Authors:  Jakub Piotr Fichna; Aleksandra Maruszak; Cezary Żekanowski
Journal:  J Appl Genet       Date:  2018-09-10       Impact factor: 3.240

4.  Stroke and Stroke-like Episodes in Muscle Disease.

Authors:  Josef Finsterer
Journal:  Open Neurol J       Date:  2012-05-18

5.  Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy.

Authors:  Lilli Winter; Matthias Türk; Patrick N Harter; Michel Mittelbronn; Cornelia Kornblum; Fiona Norwood; Heinz Jungbluth; Christian T Thiel; Ursula Schlötzer-Schrehardt; Rolf Schröder
Journal:  Acta Neuropathol Commun       Date:  2016-04-27       Impact factor: 7.801

6.  Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center.

Authors:  Yue-Bei Luo; Yuyao Peng; Yuling Lu; Qiuxiang Li; Huiqian Duan; Fangfang Bi; Huan Yang
Journal:  Front Neurol       Date:  2020-09-15       Impact factor: 4.003

  6 in total

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