Source:http://linkedlifedata.com/resource/pubmed/id/10441697
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1999-9-2
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pubmed:abstractText |
An 11-month-old Turkish female infant with Weaver syndrome together with atrial septal defect and patent ductus arteriosus which was operated successfully is reported. Weaver syndrome is a very rare disorder of unknown etiology characterized by accelerated growth of prenatal onset, advanced osseous maturation, special craniofacial features, umbilical hernia, and hoarse low-pitched cry. Congenital cardiac defect is not a usual finding. The presented case is the first reported child with Weaver syndrome in the literature operated for a congenital cardiac defect.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0172-0643
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
375-6
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pubmed:dateRevised |
2008-2-20
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pubmed:meshHeading |
pubmed-meshheading:10441697-Abnormalities, Multiple,
pubmed-meshheading:10441697-Craniofacial Abnormalities,
pubmed-meshheading:10441697-Ductus Arteriosus, Patent,
pubmed-meshheading:10441697-Female,
pubmed-meshheading:10441697-Fingers,
pubmed-meshheading:10441697-Heart Septal Defects, Atrial,
pubmed-meshheading:10441697-Hernia, Umbilical,
pubmed-meshheading:10441697-Humans,
pubmed-meshheading:10441697-Hyperostosis,
pubmed-meshheading:10441697-Infant, Newborn,
pubmed-meshheading:10441697-Syndrome
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pubmed:articleTitle |
A case with Weaver syndrome operated for congenital cardiac defect.
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pubmed:affiliation |
Department of Thoracic and Cardiovascular Surgery, Hacettepe University Medical Faculty, TR-06100 Sihhiye, Ankara, Turkey.
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pubmed:publicationType |
Journal Article,
Case Reports
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