Case Reports in Medicine

Case Reports in Medicine / 2019 / Article

Case Report | Open Access

Volume 2019 |Article ID 1384139 |

Annejet Heida, Lisette J. M. E. van der Does, Ahmed A. Y. Ragab, Natasja M. S. de Groot, "A Rare Case of the Digenic Inheritance of Long QT Syndrome Type 2 and Type 6", Case Reports in Medicine, vol. 2019, Article ID 1384139, 4 pages, 2019.

A Rare Case of the Digenic Inheritance of Long QT Syndrome Type 2 and Type 6

Academic Editor: Alexander Bauer
Received25 Jan 2019
Revised11 Apr 2019
Accepted23 May 2019
Published20 Jun 2019


We report a 37-year-old woman with an out-of-hospital cardiac arrest caused by ventricular fibrillation due to digenic inheritance of long QT syndrome type 2 (KCNH2 gene) and type 6 (KCNE2 gene). During hospitalization, prolonged QTc intervals and frequent episodes of ventricular tachyarrhythmias manifested. Genetic testing identified a mutation of the KCNH2 gene and an unclassified variant, most likely pathogenic, of the KCNE2 gene. This digenic inheritance is extremely rare.

1. Introduction

In the past decennia, our knowledge of the genetic etiology of cardiac arrhythmias has enormously increased. Cardiac tachyarrhythmias may be caused by several hereditary diseases including primary electrical disorders, such as long QT syndrome (LQTS) [1]. The LQTS is characterized by a prolongation of cardiac repolarization (QTc >450 ms in men and >460 ms in women), leading to ventricular tachyarrhythmias such as torsade des pointes (TdP). Consequently, affected patients have an increased risk of syncope and sudden cardiac death (SCD). The genes that are associated with LQTS include KCNQ1 (LQT1), KCNH2 (LQT2), SCNA5 (LQT3), KCNE1 (LQT5), and KCNE2 (LQT6) in addition to a few less frequent subtypes [2]. The most frequent variants of LQTS involve the KCNQ1, the KCNH2, and the SCN5A genes which account for approximately 90% of genotype-positive patients. Less frequent variants of LQTS involve the KCNE1 and KCNE2 genes [3, 4]. This case report is to our knowledge the first to describe the digenic inheritance of long QT syndrome type 2 (KCNH2 gene) and type 6 (KCNE2 gene).

2. Case Report

A 37-year-old Iraqi woman, living in the Netherlands, with no cardiac history, was brought to the emergency department with an out-of-hospital cardiac arrest (OHCA) due to ventricular fibrillation (VF). That evening, she had suddenly collapsed without any warnings. After two to three minutes, the police started with basic life support, and the paramedics arrived after ten minutes. On arrival, VF was documented, and after three direct current shocks, sinus rhythm was restored.

She was a nonsmoker, and there was no history of drug abuse. Current medications included diclofenac, mebeverine, and vitamin supplements. Her medical history consisted of a gastric banding operation one year ago, and prior to the event, she had only experienced some dizziness at times. The postoperative course of the gastric banding operation was uncomplicated. Her mother and four siblings lived in different countries around the world, so there was limited information about her family history. Her father passed away at the age of 55 due to complications of diabetes mellitus. The only thing that is known is that her family history was negative for SCD or cardiac disorders. Both of her sons had been diagnosed with autism but were in good physical health. The 12-lead electrocardiogram at presentation showed sinus rhythm with a frequency of 103 beats per minute and frequent premature ventricular complexes in bigeminy pattern with a QTc interval of 419 ms (Figure 1). A computed tomography (CT) scan of the thorax and cerebrum showed no evident abnormalities. After therapeutic hypothermia of 24 hours, she regained consciousness with reasonable neurological recovery without apparent sequela. Furthermore, a transthoracic echocardiogram demonstrated a good left and right ventricular function and no valvular abnormalities.

Days after detubation, episodes of frequent premature beats, nonsustained ventricular tachycardias, and prolonged QTc intervals manifested, and treatment with propranolol was started. Furthermore, frequent episodes of torsade des pointes were observed (Figure 2). Cordarone was given, which resulted in progression of the torsade des pointes into VF requiring electrical cardioversion. Cordarone treatment was discontinued. Laboratory tests showed a mild hyponatremia of 134 mmol/l, a hypokalemia of 3.1 mmol/l, and a normal calcium level of 2.38 mmol/l. However, after electrolyte corrections, ventricular tachyarrhythmias persisted. During hospitalization, the QTc interval varied between normal (<460 ms) and severely prolonged (552 ms) (Figure 3). Due to bradycardias, treatment with propranolol was discontinued. Eventually, sinus rhythm was achieved with flecainide. Coronary angiography showed no coronary artery stenosis, and cardiac magnetic resonance imaging also revealed no abnormalities.

A dual-chamber implantable cardioverter-defibrillator was implanted for secondary prevention. Subsequently, genetic testing for the LQT1, LQT2, LQT3, LQT5, and LQT6 genes identified a heterozygous c.3092_3096dup (p.Arg1033ValfsX26) mutation of the KCNH2 gene (LQT2) and a heterozygous c.170T > C (p.Ile57Thr) unclassified variant (UV) of the KCNE2 gene (LQT6). The UV (missense mutation) of the KCNE2 gene is likely a pathogenic mutation, what results in the digenic inheritance of LQT2 and LQT6. Genetic screening revealed that both sons are not carrying the familial KCNH2 mutation. They have not been tested for the UV of the KCNE2 gene.

3. Discussion

This case report describes a patient with an OHCA due to VF with the coexistence of a mutation in the KCNH2 gene (LQT2) and an UV of the KCNE2 gene (LQT6). An UV is a genetic sequence whose association with, in this case, LQTS is uncertain. In uncertain negative results, these UVs have not been found in affected counselees at high risk of LQTS. This is presumably the reason why both sons have not been tested for the UV of the KCNE2 gene. Prior studies reported that this KCNE2 UV is most likely a pathogenic mutation because it was not present in 1300 healthy controls, it causes spontaneous and drug-induced prolongation of cardiac repolarization, and it has a loss-of-function effect on the Ikr current [3, 57]. The KCNH2 and KCNE2 genes both encode the Ikr channel, but for different subunits. The KCNH2 gene encodes the HERG subunits and the KCNE2 gene the MiRP1 subunit. It was found that the MiRP1 mutants and the HERG mutants both form channels that conduct diminished potassium currents [58]. These data indicate that these two mutations combined might have an aggravating effect on loss of function of the Ikr channel.

Patients with digenic mutations are relatively common. Studies showed that in 4.6% to approximately 10.0% of the LQTS patients, two mutations were found [4, 9, 10]. To our knowledge, the coexistence of mutations in the LQT2 and LQT6 has never been described before. Mutations in the KCNH2 gene are common and often involved in the digenic inheritance of LQTS. However, LQTS is in <1% caused by mutations in the KCNE2 gene: Tester et al. found only one KCNE2 mutation in 541 unrelated patients [4]. The coexistence of LQT2 and LQT6 in one individual is thus extremely rare.

Patients with two or more mutations were more likely to have a severe clinical manifestation of LQTS. The QTc intervals were longer, and patients had more often cardiac arrhythmias and symptoms such as syncope and cardiac arrest [9, 10]. Furthermore, the onset of cardiac events in digenic inheritance is at a significantly younger age (10 ± 8 years vs 18 ± 16 years) [11]. However, our patient was 37 years old when she experienced her first cardiac event. The late presentation could be related to the fact that this KCNE2 UV in an isolated setting has not previously been associated with severe clinical manifestations, only a prolonged QT duration [12, 13]. A severe phenotype of this UV has only been described in combination with LQT3 in patients presenting with neonatal seizures and ventricular tachycardia [13]. Perhaps, exacerbation of symptoms for this KCNE2 UV is solely triggered in susceptible situations, for example, use of drugs that inhibit cardiac potassium channels [6]. In digenic inheritance, the variant may therefore have a subordinate role and cause no aggravating phenotypic expression over the single LQTS mutation. The findings of Westenskow et al. and Schwartz et al. are based on other combinations of digenic mutations, and the clinical expression of the combination of LQT2 and LQT6 is not yet described and may differ. In addition, the disease course of this patient can also be attributed to the variable penetrance of LQTS. She had, however, experienced dizziness prior to the event, which may indicate she had unconsciously suffered from TdP.

Nevertheless, it is possible that the combination of LQT2/LQT6 occurs more frequently than reported. Because most genotype-positive patients have a mutation in KCNQ1, KCNH2, or SCNA5 genes, it was recommended only to test these genes [14, 15]. However, in our case, mutations in other LQT genes could have been missed. Consequently, a potential (second) mutation will be left undiagnosed in the patient and family members. Because of the relatively high prevalence and predictive value of digenic mutations, screening of all the LQTS genes should be considered in every patient. As a result, there will be an increased risk of finding UVs which may give distress because of its uncertainty. However, if a patient carries a heterozygous mutation in two different genes, the risk that a child inherits both mutations is 25%, which implicates a more severe phenotype requiring close follow-up. By not screening all the LQTS genes, this would be missed. Napolitano et al. showed that, contrary to common perception, at least 88% of the LQTS patients have inherited the disease [14]. This states the importance of genetic screening of family members of LQTS patients as well. Furthermore, genetic screening will provide more information about the clinical presentation and incidence of the coexistence of LQT2 and LQT6.

4. Conclusion

The coexistence of long QT syndrome type 2 (KCNH2 gene) and type 6 (KCNE2 gene) is extremely rare. Screening of all the long QT syndrome genes should be considered in every patient and family member to not leave a potential (second) mutation undiagnosed.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

AH was involved in drafting the article and data collection/interpretation. LD, AR, and NG were involved in data interpretation and critical revision of the article. All authors approved the final version of the article.


  1. M. Cerrone and S. G. Priori, “Genetics of sudden death: focus on inherited channelopathies,” European Heart Journal, vol. 32, no. 17, pp. 2109–2118, 2011. View at: Publisher Site | Google Scholar
  2. N. H. Robin, P. B. Tabereaux, R. Benza, and B. R. Korf, “Genetic testing in cardiovascular disease,” Journal of the American College of Cardiology, vol. 50, no. 8, pp. 727–737, 2007. View at: Publisher Site | Google Scholar
  3. J. D. Kapplinger, D. J. Tester, B. A. Salisbury et al., “Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test,” Heart Rhythm, vol. 6, no. 9, pp. 1297–1303, 2009. View at: Publisher Site | Google Scholar
  4. D. J. Tester, M. L. Will, C. M. Haglund, and M. J. Ackerman, “Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing,” Heart Rhythm, vol. 2, no. 5, pp. 507–517, 2005. View at: Publisher Site | Google Scholar
  5. G. W. Abbott, F. Sesti, I. Splawski et al., “MiRP1 forms Ikr potassium channels with HERG and is associated with cardiac arrhythmia,” Cell, vol. 97, no. 2, pp. 175–187, 1999. View at: Publisher Site | Google Scholar
  6. F. Sesti, G. W. Abbott, J. Wei et al., “A common polymorphism associated with antibiotic-induced cardiac arrhythmia,” Proceedings of the National Academy of Sciences, vol. 97, no. 19, pp. 10613–10618, 2000. View at: Publisher Site | Google Scholar
  7. D. Isbrandt, P. Friederich, A. Solth et al., “Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics,” Journal of Molecular Medicine, vol. 80, no. 8, pp. 524–532, 2002. View at: Publisher Site | Google Scholar
  8. M. E. Curran, I. Splawski, K. W. Timothy, G. M. Vincen, E. D. Green, and M. T. Keating, “A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome,” Cell, vol. 80, no. 5, pp. 795–803, 1995. View at: Publisher Site | Google Scholar
  9. P. Westenskow, I. Splawski, K. W. Timothy, M. T. Keating, and M. C. Sanguinetti, “Compound mutations—a common cause of severe long-QT syndrome,” Circulation, vol. 109, no. 15, pp. 1834–1841, 2004. View at: Publisher Site | Google Scholar
  10. P. J. Schwartz, S. G. Priori, and C. Napolitano, “How really rare are rare diseases?:,” Journal of Cardiovascular Electrophysiology, vol. 14, no. 10, pp. 1120-1121, 2003. View at: Publisher Site | Google Scholar
  11. H. Itoh, W. Shimizu, K. Hayashi et al., “Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study,” Heart Rhythm, vol. 7, no. 10, pp. 1411–1418, 2010. View at: Publisher Site | Google Scholar
  12. P. J. Schwartz, M. Stramba-Badiale, L. Crotti et al., “Prevalence of the congenital long-QT syndrome,” Circulation, vol. 120, no. 18, pp. 1761–1767, 2009. View at: Publisher Site | Google Scholar
  13. S. E. Heron, M. Hernandez, C. Edwards et al., “Neonatal seizures and long QT syndrome: a cardiocerebral channelopathy?” Epilepsia, vol. 51, no. 2, pp. 293–296, 2010. View at: Publisher Site | Google Scholar
  14. C. Napolitano, S. G. Priori, P. J. Schwartz et al., “Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice,” JAMA, vol. 294, no. 23, pp. 2975–2980, 2005. View at: Publisher Site | Google Scholar
  15. M. J. Ackerman, S. G. Priori, S. Willems et al., “HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies,” Heart Rhythm, vol. 8, no. 8, pp. 1308–1339, 2011. View at: Publisher Site | Google Scholar

Copyright © 2019 Annejet Heida et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly as possible. We will be providing unlimited waivers of publication charges for accepted research articles as well as case reports and case series related to COVID-19. Review articles are excluded from this waiver policy. Sign up here as a reviewer to help fast-track new submissions.