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Wolff-Parkinson-White syndrome presenting in a 4.5-month-old infant with multiple accessory conduction pathways supports the hypothesis that the syndrome is congenital in origin.
This case report of a 4.5-month-old infant with WPW syndrome supports the hypothesis that the condition is congenital in origin.
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Infant case supports congenital WPW origin; leaves open confirmation in larger prospective studies.
A case of Wolff-Parkinson-White syndrome in an infant 4½ months of age with electrocardiographic findings suggestive of several congenital accessory conduction pathways is presented. The age of the patient and the findings lend support to the hypothesis that this syndrome is congenital in origin.
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Richmond et al. (1948) studied this question. Wolff-Parkinson-White syndrome presenting in a 4.5-month-old infant with multiple accessory conduction pathways supports the hypothesis that the syndrome is congenital in origin.
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