Publication:
Case report and review: prenatal diagnosis of congenital megalourethra.

dc.contributor.authorPatama Promsonthien_US
dc.contributor.authorWit Viseshsindhen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-24T09:36:14Z
dc.date.available2018-09-24T09:36:14Z
dc.date.issued2010-01-01en_US
dc.description.abstractMegalourethra is a rare congenital anomaly characterized by dilatation of the penile urethra which causes functional obstruction of the lower urinary system. We present a case of congenital megalourethra diagnosed prenatally. Transabdominal sonography revealed a male fetus with bilateral hydroureter, hydronephrosis, dilated bladder and normal amniotic fluid. The fetal penis was enlarged and the penile urethra was dilated with ballooning at the distal end. The urethral meatus was identified. The fetus was delivered at term with a favorable outcome. Copyright (c) 2010 S. Karger AG, Basel.en_US
dc.identifier.citationFetal diagnosis and therapy. Vol.28, No.2 (2010), 123-128en_US
dc.identifier.doi10.1159/000316929en_US
dc.identifier.issn14219964en_US
dc.identifier.other2-s2.0-85027952303en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/29835
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85027952303&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleCase report and review: prenatal diagnosis of congenital megalourethra.en_US
dc.typeReviewen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85027952303&origin=inwarden_US

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