Journals / Medical Research Reports / 2018 / Cilt: 1 - Sayı: 1

A RARE COMBINATION: BIVENTRICULAR NON-COMPACTION, EBSTEIN’S ANOMALY, WOLF PARKINSON WHITE SYNDROME AND MITRAL VALVE PROLAPSUS

Pages
20–22
Publication Date
2018-08-13
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The combination of these congenital abnormalities could infer a common genetic predisposition with different presentation of myocardium and leaflets.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Ventricular non-compaction and Ebstein’s anomaly are 2 rare congenital abnormalities.
📊
Key Findings & Data:We report a case of 25-year old male patient with biventricular non-compaction, Ebstein’s anomaly, mitral valve prolapsus and Wolf-Parkinson-White syndrome.
💡
Conclusion & Impact:The combination of these congenital abnormalities could infer a common genetic predisposition with different presentation of myocardium and leaflets.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Biventricular non-compaction · Ebstein’s Anomaly · Wolf Parkinson White Syndrome

Abstract

Ventricular non-compaction and Ebstein’s anomaly are 2 rare congenital abnormalities. In some cases both abnormalities share common genetic predisposition. Both abnormalities could be associated. We report a case of 25-year old male patient with biventricular non-compaction, Ebstein’s anomaly, mitral valve prolapsus and Wolf-Parkinson-White syndrome. The combination of these congenital abnormalities could infer a common genetic predisposition with different presentation of myocardium and leaflets.

🔖

Cite This Article

ULUGANYAN, M., BAKHSHALİYEV, N., ENHOŞ, A., AY, N. K. (2018). A RARE COMBINATION: BIVENTRICULAR NON-COMPACTION, EBSTEIN’S ANOMALY, WOLF PARKINSON WHITE SYNDROME AND MITRAL VALVE PROLAPSUS. Medical Research Reports, Cilt: 1 - Sayı: 1, 20–22. https://ajindex.com/articles/789954

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (9)

  1. Budde BS, Binner P, Waldmuller S, et al. Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene. PLoS ONE 2007 2:e1362
  2. Sinkovec M, Kozelj M, Podnar T. Familial biventricular myocardial non-compaction associated with Ebstein’s malformation. Int J Cardiol 2005;102:297-302
  3. Attenhofer Jost CH, Connolly HM, O’Leary PW, et al. Left heart lesions in patients with Ebstein’s anomaly. Mayo Clin Proc 2005;80:361-368
  4. Saltik L, Eroglu E, Bayrak F, et al. Left ventricular non-compaction associated with Ebstein’s anomaly. Turk Kardiyol Dern Ars 2009;37:269-272
  5. Baysan O, Yokusoglu M, Bugan B, et al. E-page original images. A case of Ebstein’s anomaly and biventricular non-compaction. Anadolu Kardiyol Derg 2010;10:E26
  6. Captur G, Nihoyannopoulos P. Left ventricular non-compaction: Genetic heterogeneity, diagnosis and clinical course. Int J Cardiol 2010;140:145–153
  7. Towbin JA, Lorts A, Jefferies JL. Left ventricular non-compaction cardiomyopathy. Lancet 2015;386:813–825
  8. Stahli BE, Gebhard C, Biaggi P, et al. Left ventricular non-compaction: Prevalence in congenital heart disease. Int J Cardiol 2013;167:2477–2481
  9. Kelle AM, Bentley SJ, Rohena LO, et al. Ebstein anomaly, left ventricular non-compaction, and early onset heart failure associated with a de novo α-tropomyosin gene mutation. Am J Med Genet A. 2016;170:2186-2190.