neonatal ovarian cysts (noc) are usually self-limiting structures, however, large or complex cysts may lead to severe complications. unfortunately, no standard guidelines have been introduced for the management, treatment and follow-up of these cysts. in this report, we aimed to introduce a very large noc without any pre- and post-natal complications. a 30 year-old mother, gravida 2, para 2, wi...

background evaluation of the cerebellum and vermis is one of the integral parts of the fetal cranial anomaly screening. objectives the aim of this study was to create a nomogram for fetal vermis measurements between 17 and 30 gestational weeks. patients and methods this prospective study was conducted on 171 volunteer pregnant women between march 2013 and december 2014. measurements of the feta...

in previous years, identification of fetal cells in maternal blood circulation has caused a new revolution in non-invasive method of prenatal diagnosis. low number of fetal cells in maternal blood and long-term survival after pregnancy limited the use of fetal cells in diagnostic and clinical applications. with the discovery of cell-free fetal dna (cffdna) in plasma of pregnant women, access to...

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, ambiguous...

Background: Prenatal diagnosis for Fetal Chromosomal anomalies currently relies on assessment of risk followed by a combination of biochemical and nuchal translucency. Trisomy 21 is the most common trisomy that is associated with intellectual disability. Pregnant women who receive a prenatal diagnosis of trisomy 21 currently have the option of continuing or terminating their pregnancy, but no f...

down syndrome (ds) is a birth defect with huge medical and social costs, caused by trisomy of whole or part of chromosome 21. it is the most prevalent genetic disease worldwide and the common genetic cause of intellectual disabilities appearing in about 1 in 400-1500 newborns. although the syndrome had been described thousands of years before, it was named after john langdon down who described ...

Objetivo: Analizar los controles prenatales insuficientes en adolescentes primigestas. Método: Descriptiva observacional. Resultados: El 25% de primigestas dicen conocer os riesgos que se pueden presentar por no asistir al Control Prenatal es la presencia traumatismos nacer él bebé. Conclusión: Concientizar a las mediante asistencia del control prenatal, reduciendo así complicaciones ponen ries...

BACKGROUND The need to provide high quality prenatal care services, which take account of women's views and specifically address their need for information, support and communication, has been advocated and group prenatal care, had been suggested as one of the ways to achieve this objective. The purpose of this study was to examine the impact of group versus individual prenatal care on satisfac...