Prenatal diagnosis of unilateral dacryocystocele: A rare case report

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Prenatal early diagnosis of dacryocystocele, a case report and review of literature.

Dacryocystocele (mucocele, amniocele) is a relatively rare variant of nasolacrimal duct obstruction which refers to the cystic dilatation of lacrimal pathway above and below the lacrimal sac. It is a benign pathology and can be treated successfully after birth, but its prenatal detection is important, because it may be seen in numerous syndromes and may serve as their marker. Bilateral cysts ha...

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Prenatal diagnosis of lissencephaly: A case report.

INTRODUCTION Lissencephaly ("smooth brain") forms a major group of brain malformations due to abnormal neuronal migration. It can cause severe intellectual and motor disability and epilepsy in children. The prenatal diagnosis of this malformation is rare. CASE REPORT We presented a case of the prenatal diagnosis of lissencephaly. A 30-year-old pregnant woman was reffered to the hospital at th...

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Dacryocystocele on prenatal ultrasonography: diagnosis and postnatal outcomes

PURPOSE To report the incidence of dacryocystoceles detected by prenatal ultrasonography (US) and their postnatal outcomes and to determine the factors associated with the postnatal persistence of dacryocystoceles at birth. METHODS We retrospectively reviewed the prenatal US database at our institution for the period between January 2012 and December 2013. The medical records of women who had...

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Prenatal diagnosis and postnatal findings of cloacal malformation: a case report

Introduction: Cloacal malformation is an extremely rare fetal pathological condition but an important anomaly that presents as a variety of defects. It predominantly affects females, with prevalence of 1 in 50,000 births. Prenatal ultrasonography usually showed oligohydramnios and the fetus having a large cystic mass in the lower abdomen with a single septum, bilateral hydronephrosis, ambig...

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ژورنال

عنوان ژورنال: Cumhuriyet Medical Journal

سال: 2019

ISSN: 1305-0028

DOI: 10.7197/223.vi.487385