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dc.contributor.authorSomsri Pitukkijronnakornen_US
dc.contributor.authorPatama Promsonthien_US
dc.contributor.authorPanyu Panburanaen_US
dc.contributor.authorRasig Rangsiprakarnen_US
dc.contributor.authorApichart Chittacharoenen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-12T02:36:48Z-
dc.date.available2018-07-12T02:36:48Z-
dc.date.issued2008-11-01en_US
dc.identifier.citationJournal of the Medical Association of Thailand. Vol.91, No.11 (2008), 1651-1655en_US
dc.identifier.issn01252208en_US
dc.identifier.issn01252208en_US
dc.identifier.other2-s2.0-57149096263en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=57149096263&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/19473-
dc.description.abstractObjective: To evaluate the accuracy of prenatal ultrasonographic diagnosis in fetuses with trisomy 13. Material Method: The present study consisted of all fetuses diagnosed of trisomy 13 and delivered at Ramathibodi Hospital between 1997 and 2006. Results: There were 15 cases of trisomy 13. Twelve cases (80.0%) were detected by prenatal ultrasonographic examination, and 3 cases (20.0%) were missed. Mean maternal age was 31.4 years old. Sixty-six percent were diagnosed in 2nd trimester (mean 19.4 weeks). The earliest gestational age for detection was 12 weeks 6 days. The most common abnormal ultrasonographic findings were holoprosencephaly (46.7%), and facial defects (40.0%). Conclusion: The accuracy of prenatal sonographic diagnosis in trisomy 13 fetuses was 80%. The most sensitive prenatal ultrasonographic findings in trisomy 13 were holoprosencephaly and facial defects.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=57149096263&origin=inwarden_US
dc.subjectMedicineen_US
dc.titlePrenatal ultrasonographic findings in "trisomy 13"en_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
Appears in Collections:Scopus 2006-2010

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