1987
DOI: 10.1016/0002-9149(87)91177-5
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Frequency, diagnosis and clinical characteristics of patients with multiple accessory atrioventricular pathways

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Cited by 86 publications
(28 citation statements)
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“…There were also certain preferred groupings of pathway locations in structural disease patients with multAP, most notably a TV + S combination in Ebstein’s malformation. 22 A genetic mutation affecting AV valve development could explain these observations. For example, the Nkx2.5/Alk3/BMPR pathway is involved in AV patterning and electrically-insulating annulus fibrosis formation.…”
Section: Discussionmentioning
confidence: 99%
“…There were also certain preferred groupings of pathway locations in structural disease patients with multAP, most notably a TV + S combination in Ebstein’s malformation. 22 A genetic mutation affecting AV valve development could explain these observations. For example, the Nkx2.5/Alk3/BMPR pathway is involved in AV patterning and electrically-insulating annulus fibrosis formation.…”
Section: Discussionmentioning
confidence: 99%
“…13 Humans affected by an Ebstein anomaly may have multiple APs that are typically located in the right free wall or in the posterior part of the septum, locations that are more frequently described in dogs. 14,15 Most dogs that have APs are Labrador Retrievers and Boxers, suggesting a possible predisposition of these breeds to develop anomalous atrioventricular bundle connections. 2,13,16 In humans, APs allow antegrade and retrograde conduction with an all-or-none pattern.…”
Section: Discussionmentioning
confidence: 99%
“…4 In around 10% of cases multiple pathways exist. 5 The incidence of associated congenital abnormalities ranges from 7% to 20%. 3 6 Tricuspid valve lesions are the most common.…”
Section: Discussionmentioning
confidence: 99%