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Fetal hydrometrocolpos, uterus didelphys with low vaginal and anal atresia: difficulties in differen...

Fetal hydrometrocolpos, uterus didelphys with low vaginal and anal atresia: difficulties in differen...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1312659590

Fetal hydrometrocolpos, uterus didelphys with low vaginal and anal atresia: difficulties in differentiation from a complex cloacal malformation: a case report

About this item

Full title

Fetal hydrometrocolpos, uterus didelphys with low vaginal and anal atresia: difficulties in differentiation from a complex cloacal malformation: a case report

Publisher

Switzerland: Éditions Médecine et Hygiène

Journal title

Genetic counseling, 2012-01, Vol.23 (4), p.513-517

Language

English

Formats

Publication information

Publisher

Switzerland: Éditions Médecine et Hygiène

More information

Scope and Contents

Contents

Hydrometrocolpos, occurring in approximately 1/6000 newborn girls, can be caused by a stenotic urogenital sinus, a severe cloacal malformation, but also by other conditions such as an imperforate hymen, a midline vaginal septum and vaginal atresia. The prenatal differential diagnosis of this wide spectrum of conditions is not easy and requires a mu...

Alternative Titles

Full title

Fetal hydrometrocolpos, uterus didelphys with low vaginal and anal atresia: difficulties in differentiation from a complex cloacal malformation: a case report

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1312659590

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1312659590

Other Identifiers

ISSN

1015-8146

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