Literature DB >> 19306361

Progression of conduction system disease in a paced patient with Kearns-Sayre syndrome.

Murat Yeşil1, Serdar Bayata, Nursen Postaci, Erdinç Arikan.   

Abstract

The Kearns-Sayre syndrome is a rare condition characterized by external ophthalmoplegia, retinal pigmentary degeneration and progressive impairment of cardiac conduction. We report a patient with the permanent pacemaker. The spontaneous cardiac impulse formation disappeared during long-term follow-up in this patient with Kearns-Sayre Syndrome. 2009 Wiley Periodicals, Inc.

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Year:  2009        PMID: 19306361      PMCID: PMC6653339          DOI: 10.1002/clc.20242

Source DB:  PubMed          Journal:  Clin Cardiol        ISSN: 0160-9289            Impact factor:   2.882


  2 in total

1.  Cardiac arrest in kearns-sayre syndrome.

Authors:  Ingrid van Beynum; Eva Morava; Marjan Taher; Richard J Rodenburg; Judit Karteszi; Kalman Toth; Eszter Szabados
Journal:  JIMD Rep       Date:  2011-09-06

2.  Dilated cardiomyopathy with cardiogenic shock in a child with Kearns-Sayre syndrome.

Authors:  Swati Sehgal; Swati Choudhry; Larisa Debelenko; Thomas L'Ecuyer
Journal:  BMJ Case Rep       Date:  2016-02-16
  2 in total

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