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Case Reports
. 2018 Dec 18;5(3):169-172.
doi: 10.1016/j.hrcr.2018.12.004. eCollection 2019 Mar.

Appropriate use of genetics in a young patient with atrioventricular block and family history of sudden cardiac death

Johnni Rudbeck-Resdal  1   2 , Jens Cosedis Nielsen  1   2 , Henning Bundgaard  3 , Henrik K Jensen  1   2
Affiliations
Case Reports

Appropriate use of genetics in a young patient with atrioventricular block and family history of sudden cardiac death

Johnni Rudbeck-Resdal et al. HeartRhythm Case Rep. .
No abstract available

Keywords: Aborted sudden cardiac death; Atrioventricular block; Genetic; ICD; LMNA; Lamin A/C.

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Figures

Figure 1
Figure 1
Family pedigree. The arrow points to the index case.
Figure 2
Figure 2
Twelve-lead electrocardiogram with advanced atrioventricular block.
Figure 3
Figure 3
Recordings from cardiac resynchronization therapy device with ventricular fibrillation (VF) and successful implantable cardioverter-defibrillator shock therapy.
See this image and copyright information in PMC

References

    1. Danish Pacemaker and ICD Register. Danish Pacemaker and ICD Register - Annual report. 2015. https://ssl.icddata.dk/download/Danish_Pacemaker_and_ICD_Register_Annual... Available at. Accessed April 10, 2018.
    1. Fatkin D., MacRae C., Sasaki T. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N Engl J Med. 1999;341:1715–1724. - PubMed
    1. Kumar S., Baldinger S.H., Gandjbakhch E. Long-term arrhythmic and nonarrhythmic outcomes of lamin A/C mutation carriers. J Am Coll Cardiol. 2016;68:2299–2307. - PubMed
    1. Dittmer T.A., Misteli T. The lamin protein family. Genome Biol. 2011;12:222. - PMC - PubMed
    1. Rankin J., Ellard S. The laminopathies: a clinical review. Clin Genet. 2006;70:261–274. - PubMed

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