Source:http://linkedlifedata.com/resource/pubmed/id/11175485
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2001-2-22
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pubmed:abstractText |
Syncope in children is primarily related to vagal hyperreactivity, but ventricular tachycardia (VT) way rarely be seen. Catecholaminergic polymorphic VT is a rare entity that can occur in children without heart disease and with a normal QT interval, which may cause syncope and sudden cardiac death. In this report, we describe the clinical features, treatment, and clinical follow-up of three children with syncope associated with physical effort or emotion and catecholaminergic polymorphic VT. Symptoms were controlled with beta-blockers, but one patient died suddenly in the fourth year of follow-up. Despite the rare occurrence, catecholaminergic polymorphic VT is an important cause of syncope and sudden death in children with no identified heart disease and normal QT interval.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0066-782X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
76
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
63-74
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:11175485-Adrenergic beta-Antagonists,
pubmed-meshheading:11175485-Child,
pubmed-meshheading:11175485-Death, Sudden, Cardiac,
pubmed-meshheading:11175485-Electrocardiography,
pubmed-meshheading:11175485-Female,
pubmed-meshheading:11175485-Follow-Up Studies,
pubmed-meshheading:11175485-Humans,
pubmed-meshheading:11175485-Nadolol,
pubmed-meshheading:11175485-Syncope,
pubmed-meshheading:11175485-Tachycardia, Ventricular
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pubmed:year |
2001
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pubmed:articleTitle |
Catecholaminergic polymorphic ventricular tachycardia. An important diagnosis in children with syncope and normal heart.
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pubmed:affiliation |
Paulista School of Medicine, São Paulo Federal University, São Paulo, SP, Brazil.
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pubmed:publicationType |
Journal Article,
Case Reports
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