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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
1993-2-24
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pubmed:abstractText |
A rare vascular portohepatic anomaly was identified in a Down syndrome patient with a 47,XY,-2,+der(2),+der(21)t(2;21)(p13;q22.1) mat chromosomal complement. This vascular defect involves a direct communication between the right portal vein and the inferior vena cava (IVC). We discuss the possibility that this vascular defect is a rare manifestation in Down syndrome. Alternatively, the existence of these 2 rare events in the same patient raises the possibility that they are causally related.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0148-7299
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
44
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
288-92
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:1488975-Chromosomes, Human, Pair 2,
pubmed-meshheading:1488975-Chromosomes, Human, Pair 21,
pubmed-meshheading:1488975-Down Syndrome,
pubmed-meshheading:1488975-Ductus Arteriosus,
pubmed-meshheading:1488975-Echocardiography,
pubmed-meshheading:1488975-Fistula,
pubmed-meshheading:1488975-Humans,
pubmed-meshheading:1488975-Infant, Newborn,
pubmed-meshheading:1488975-Liver,
pubmed-meshheading:1488975-Male,
pubmed-meshheading:1488975-Portal Vein,
pubmed-meshheading:1488975-Translocation, Genetic,
pubmed-meshheading:1488975-Trisomy,
pubmed-meshheading:1488975-Vena Cava, Inferior
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pubmed:year |
1992
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pubmed:articleTitle |
Portohepatic shunt in a Down syndrome patient with an interchange trisomy 47,XY,-2,+der(2),+der(21)t(2;21)(p13;q22.1)mat.
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pubmed:affiliation |
Department of Pediatrics, Montreal Children's Hospital, Quebec, Canada.
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pubmed:publicationType |
Journal Article,
Case Reports
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