2019
DOI: 10.1155/2019/1061065
|View full text |Cite
|
Sign up to set email alerts
|

Hypertrophic Cardiomyopathy and Wolff-Parkinson-White Syndrome in a Young African Soldier with Recurrent Syncope

Abstract: Syncope is a common manifestation of both hypertrophic cardiomyopathy (HCM) and Wolff-Parkinson-White (WPW) syndrome. The most common arrhythmia in HCM is ventricular tachycardia (VT) and atrial fibrillation (AF). While preexcitation provides the substrate for reentry and supraventricular tachycardia (SVT), AF is more common in patients with preexcitation than the general population. Concurrence of HCM and WPW has been reported in many cases, but whether the prognosis or severity of arrhythmia is different com… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4

Citation Types

0
4
0

Year Published

2023
2023
2023
2023

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(4 citation statements)
references
References 9 publications
0
4
0
Order By: Relevance
“…Of the predicted P/LP variants on the ACMG SFv3.0, a pathogenic variant of PRKAG2 was identified in two individuals. Variants in PRKAG2 are associated with the autosomal dominantly inherited Wolff Parkinson White Pattern(WPWP) (Chhabraetal.,2023).WPWPisacongenitalanomalyaffectingthenormalconductionoftheelectricalimpulsesbetweentheatriaandventricles.Commonly associatedsymptomsincludechestpain,palpitations,progressive shortness of breath, syncope and, in rare cases, suddencardiacdeath (Talleetal., 2019).Theinformation on the epidemiology of WPW has been limited in sub-SaharanAfricabyinadequateresources,diagnosticequipment and screening programs (Ogunlade & Asafa, 2017;Talle et al, 2019). A prevalence of 0.11% in Nigeria was reportedinacohortofyoungadultsaged15-40 (Ogunlade & Asafa, 2017).…”
Section: Discussionmentioning
confidence: 99%
See 3 more Smart Citations
“…Of the predicted P/LP variants on the ACMG SFv3.0, a pathogenic variant of PRKAG2 was identified in two individuals. Variants in PRKAG2 are associated with the autosomal dominantly inherited Wolff Parkinson White Pattern(WPWP) (Chhabraetal.,2023).WPWPisacongenitalanomalyaffectingthenormalconductionoftheelectricalimpulsesbetweentheatriaandventricles.Commonly associatedsymptomsincludechestpain,palpitations,progressive shortness of breath, syncope and, in rare cases, suddencardiacdeath (Talleetal., 2019).Theinformation on the epidemiology of WPW has been limited in sub-SaharanAfricabyinadequateresources,diagnosticequipment and screening programs (Ogunlade & Asafa, 2017;Talle et al, 2019). A prevalence of 0.11% in Nigeria was reportedinacohortofyoungadultsaged15-40 (Ogunlade & Asafa, 2017).…”
Section: Discussionmentioning
confidence: 99%
“…WPWP is a congenital anomaly affecting the normal conduction of the electrical impulses between the atria and ventricles. Commonly associated symptoms include chest pain, palpitations, progressive shortness of breath, syncope and, in rare cases, sudden cardiac death (Talle et al, 2019 ). The information on the epidemiology of WPW has been limited in sub‐Saharan Africa by inadequate resources, diagnostic equipment and screening programs (Ogunlade & Asafa, 2017 ; Talle et al, 2019 ).…”
Section: Discussionmentioning
confidence: 99%
See 2 more Smart Citations