Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/70910
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dc.contributor.authorKuntharee Traisrisilpen_US
dc.contributor.authorSujinun Nunthapiwaten_US
dc.contributor.authorSuchaya Luewanen_US
dc.contributor.authorTheera Tongsongen_US
dc.date.accessioned2020-10-14T08:44:29Z-
dc.date.available2020-10-14T08:44:29Z-
dc.date.issued2020-01-01en_US
dc.identifier.issn10970096en_US
dc.identifier.issn00912751en_US
dc.identifier.other2-s2.0-85086410472en_US
dc.identifier.other10.1002/jcu.22882en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85086410472&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70910-
dc.description.abstract© 2020 Wiley Periodicals, Inc. This report describes a variant of McKusick-Kaufman syndrome presenting with a large fetal abdominal cyst of hydrometrocolpos at 37 weeks of gestation. The diagnosis was based on the ultrasound findings of a large homogeneous hypoechoic cyst (diameter of >10 cm) with incomplete septum, thickened wall, superiorly connecting to the dilated uterus, consistent with hydrometrocolpos. Additionally, pre-axial mirror polydactyly of the left foot was suspected. Postnatal examination/work-up confirmed the prenatal findings. This is the first report of prenatal diagnosis of hydrometrocolpos with complex polydactyly of mirror image pre-axial duplications containing nine toes instead of six-toe postaxial polydactyly.en_US
dc.subjectMedicineen_US
dc.titleFetal hydrometrocolpos with pre-axial mirror polydactyly as a new variant of McKusick-Kaufman syndromeen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Clinical Ultrasounden_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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