This study investigates neonatal outcomes in singleton and multiple pregnancies following vitro fertilization (IVF) using donor (IVF-D) versus autologous (IVF-A) material. A retrospective cohort analysis was conducted with 988 neonates born between 2017 2024 across three tertiary units Romania. The primary included preterm birth, low birthweight, asphyxia, congenital malformations. IVF-D were associated a higher prevalence of adverse outcomes, particularly gestations. Preterm birth...

The use of assisted reproductive technology has increased in Romania the past several years. Although most these pregnancies are uncomplicated, vitro fertilization is associated with an risk for adverse perinatal outcomes primarily caused by risks prematurity, gestational diabetes mellitus, and hypertensive disorders. Infertility can be a variety factors, including both male female some cases, cause remains unknown. In our clinic, etiology infertility was known cases equally distributed...

Early detection of micrognathia during prenatal care is crucial to mitigate the associated risks and prevent un­fore­seen emergencies requiring invasive procedures, like tracheo­stomy. It enables proper planning for delivery in spe­cia­lized tertiary centers staffed with experienced teams managing such cases. This proactive approach en­hances cli­ni­cian readiness, facilitates decision-making re­gar­ding ma­nage­ment strategies advance, fosters im­proved fa­mily education support. The...

Abstract Introduction Oesophageal duplication cyst (EDC) is a rare congenital anomaly representing, after neuronal tumours, the second most common cause of posterior mass in children, with prevalence approximately 1/22,500 live births. Cervical cysts are very rare, and their antenatal detection fairly uncommon. Methods We report case an isolated large mediastinal cervical tubular EDC diagnosed prenatally third trimester. Results After birth, baby became symptomatic developing respiratory...

Body stalk anomaly is a term used to describe pattern of severe defects that are incompatible with life. This con­d­ition should be suspected when encountering large ab­do­mi­nal defect, along axial skeletal abnormalities such as kyphosis or scoliosis and short absent umbilical cord. considered fatal anomaly, thus being crucial distinguish it from other anterior wall de­fects evaluating the management options. We re­port case patient diagnosed at 15 weeks ges­ta­tion complex fetal anomalies...

Background: Assisted reproductive technology (ART) nowadays plays a major role in the treatment of infertility, with most frequently used techniques being vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). The objective this study is to analyze pregnancies achieved using these ART their correlations prematurity congenital malformations rates. Methods: This an observational retrospective longitudinal that includes 814 newborns conceived through ART, namely IVF or ICSI....

Background and objectives. Preterm is defined as babies born alive before 37 weeks of pregnancy are completed. It one the world's critical health problems because it may be a significant cause long-term neurodevelopmental disability. The purpose this work was to evaluate impact premature birth brain injuries on neurological development identify soon possible in order prevent or minimize sequelae much possible. Materials methods. Between June 2022 July 2024, 374 infants were examined at...

The 22q11.2 deletion syndrome (22q11.2DS) is the most common chromosomal microdeletion disorder caused by hemizygous of long arm chromosome 22. It now known to have a heterogenous presentation that includes multiple additional congenital anomalies and later-onset conditions, such as gastrointestinal renal abnormalities, autoimmune disease, variable cognitive delays, behavioral phenotypes psychiatric illness. purpose our paper present case fetus diagnosed with rare complex cardiac...

Cystic hygroma represents fluid accumulation often cephalic on the left side, with incidence of 1/6000-1/16000. Genetic anomalies are found in 20-75% cases, most frequent Turner, Down's, Klinefelter, Edwards and Patau syndromes, but also subchromosomal – Noonan, Fryns, multiple pterygium syndrome achondroplasia. This report aims to identify correlation between cystic genetic our practice. We a small series cases diagnosed during January 2022–December 2022 Department first trimester their...

The 22q11.2 deletion syndrome (22q11.2DS) is the most common chromosomal microdeletion disorder caused by hemizygous of long arm chromosome 22. It now known to have a heterogenous presentation that includes multiple additional congenital anomalies and later-onset conditions, such as gastrointestinal renal abnormalities, autoimmune disease, variable cognitive delays, behavioral phenotypes psychiatric illness. purpose our paper present case fetus diagnosed with complex association cardiac...

Electronic poster abstractstwo nodular foci at the bifurcation of abdominal aorta and in front left iliac artery, consider aneurysmal expansion.After 38 weeks pregnancy, a boy was delivered naturally.Abdominal ultrasound examination on third day after birth showed that two adjacent anechoic regions could be detected middle lower segments aorta.The diagnosis aortic aneurysm (AAA).There no special condition follow-up newborns one month birth.Discussion: AAA definite etiology is defined as...

The optimal management of leiomyomas during caesarean delivery remains unclear, as it may be considered feasible and a safe procedure, or an absolute contraindication. Recent meta-analyses suggest that myomectomy is associated with clinical insignificant increase in ope­ra­tive time, blood loss hospital stay, especially mul­tiple large-size myomas, should taken into consideration by experienced surgeons appropriate hemostatic techniques tertiary-care centers. We present the case patient...