Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1998-9-8
pubmed:abstractText
The acardiac fetus is a rare anomaly of about 1 percent of monozygotic pregnancies, occurring in approximately 1 in 35,000 pregnancies. The special hemodynamic circumstances of the normal heart having to pump an excessive amount of blood for a long period of time will influence the chance of survival of this fetus. In two case-report with many figures pathologic-anatomical problems and prospective management to improve the outcome of monozygotic multiple pregnancies complicated by acardiac malformation were presented. The pathogenesis of metabolic dysbalance in these pregnancies was discussed.
pubmed:language
ger
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:issn
0948-2393
pubmed:author
pubmed:issnType
Print
pubmed:volume
202
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
80-5
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:articleTitle
[Monozygotic multiple pregnancies with acardiac anomalies].
pubmed:affiliation
Frauenklinik, Klinikums Schwerin.
pubmed:publicationType
Journal Article, English Abstract