Defects
- 2D strain analysis reveals biventricular dysfunction in Tetralogy of Fallot
- A 12 month review of small heads & small legs - are we over investigating?
- A case extra-lobar pulmonary sequestration of antenatal discovery
- A case lymphoma of the uterine cervix
- A case of a rare abdominal fetal cyst
- A case of an omphalocele and the many associated anomalies
- A case of challenges in categorizing prenatal multiple anatomic abnormalities in cloacal exstrophy at early gestational age
- A case of challenges of prenatal diagnosis and management of fetal dacryocystocele in Guatemala
- A case of chondrodysplasia punctata
- A case of complete unbalanced atrioventricular septal defect with right ventricular hypoplasia
- A case of Dandy Walker malformation as a manifestation of PHACE syndrome
- A case of Dandy-Walker malformation in a twin pregnancy
- A case of detection of spina bifida at 11 weeks’ ultrasound
- A case of early prenatal detection and management of thanatophoric dysplasia
- A case of ex utero intrapartum treatment in a rare craniofacial tumor
- A case of fatal complex umbilical cord anomaly
- A case of fetal atrioventricular heart block as a first manifestation of maternal connective tissue disease
- A case of fetal ovarian cyst and review of management strategies
- A case of fetal ovarian cysts with prenatal torsion
- A case of first trimester ultrasonographic approach to diagnosing Sirenomelia
- A case of from suspected clubfoot to multiple pterygium syndrome
- A case of frontal encephalocele
- A case of giant fetal sacrococcygeal teratoma
- A case of integral study in a patient with sonographic appearance of hydropic degeneration in ultrasound
- A case of klippel -Trenaunay syndrome associated with large splenic cystic lymphangioma and pregnancy
- A case of massive neck fetal lymphangioma
- A case of Meckel-Gruber syndrome in Jordan
- A case of megacystis- new polymalformative syndrome
- A case of oculoauricularfrontonasal syndrome and the importance of the combined 2D/3D Ultrasound and MRI
- A case of osteogenesis imperfecta
- A case of perinatal outcomes following conservative management of fetal bronchopulmonary sequestration
- A case of prenatal abnormal position of the gallbladder
- A case of prenatal bilateral junction syndrome
- A case of prenatal clues on Holt-Oram Syndrome
- A case of prenatal diagnosis of a complex genitourinary malformation
- A case of prenatal diagnosis of diastematomyelia
- A case of prenatal diagnosis of fetal cardiac rhabdomyoma associated with tuberous sclerosis
- A case of prenatal diagnosis of Hajdu-Cheney Syndrome
- A case of prenatal diagnosis of hemimegalencephaly
- A case of prenatal diagnosis of prune-belly syndrome
- A case of prenatal management of a major omphalocele by botulinum toxin injection
- A case of prenatal ultrasonographic diagnosis of umbilical vein varix at 36 weeks and management
- A case of recurrent meckel-gruber syndrome
- A case of reversal of severe sustained fetal supraventricular tachycardia with transplacental flecainide
- A case of saldino Noonan syndrome prenatal diagnostic
- A case of Treacher Collins syndrome, it is possible to evaluate the severity through imaging studies
- A case of ultrasound diagnosis of Chiari II malformation anomaly
- A case of unraveling the ganglionic eminence anomalies in monozygotic twin pregnancy
- A case report uncomplicated fetal ovarian cyst
- A case report urinary ascites as a rare indicator of posterior urethral valves
- A case reprot caudal regression syndrome
- A case study on Type 2 sacrococcygeal teratoma (SCT)
- A clinical perspective on cystic placental changes: insights from three unique cases
- A lethal case of amniotic band sequence and severe craniofacial malformation
- A paradigm shift: diagnosing fetal malformations on the 1st trimester ultrasound
- A rare case of craniosynostosis and suspected fontaine progeroid syndrome
- A rare case of midline developmental defect in fetal period
- A rare case of vanished gastroschisis: the role of ultrasound in delivery and surgical planning
- Abdominal wall defects: a casuistry in a district hospital
- Aberrant right subclavian artery: prenatal diagnosis and management
- Abnormal digestive images: ultrasonographic aspects and diagnoses
- Acrania-exencephaly-anencephaly sequence - regarding clinical cases
- Agenesis of the ductus venosus – three cases with favorable evolution
- AI-based standardization of fetal facial planes in 3d prenatal ultrasound: a multi-center study
- Analysing the pregnancy outcomes in fetuses diagnosed with Binder’s facies on ultrasound examination: a retrospective analysis
- Anencephaly: A case report of obstetrics and gynecology Department of Ben Arous hospital
- Antenatal diagnosis and outcome of corpus callosum agenesis
- Aortic isthmus flow characteristics throughout gestation in fetal coarctation of the aorta
- Arachnoid cysts: an uncertain prognosis
- Arnold Chiari II malformation
- Arterial and venous blood flow of bronchopulmonary sequestration in predicting fetal hydrothorax and/or hydrops
- Assessment of antenatal and postnatal surviving indexes of fetus with congenital diaphragmatic hernia
- Association between cardiovascular biomarkers in cord blood and right ventricular outflow tract obstruction severity in tetralogy of Fallot fetuses
- Associations and outcomes of prenatally detected rhombencephalosynapsis
- Bilateral fetal ovarian cyst: one simple cyst and another complex-torsioned that end-up in autoamputation
- Bladder Exstrophy diagnosis in the first trimester
- Can fetal abdominal wall defects predict postnatal outcomes?
- Can ultrasound findings predict the site of obstruction of fetal non-duodenal small bowel atresia?
- Cardiac remodeling in art-conceived singletons: a prospective cohort study comparing biopsied and non-biopsied embryos with spontaneously conceived embryos
- Case Series on prenatally detected rare cephaloceles with postnatal follow up
- Cases of screening for ventriculomegaly
- Cerebellar hypoplasia and the importance of evaluating the cerebellum in the third trimester: a case series
- Chorioangioma: an unusual prenatal diagnosis
- Chromosomal aberrations in fetuses with isolated muscular ventricular septum defects – a retrospective study and meta-analysis
- Chylothorax in the fetus: a rare intrauterine complication with significant implications for neonatal prognosis
- Clinical case of antenatally diagnosed sirenomelia
- Color Doppler patterns recognition indicative of congenital heart defects at the first trimester referral scan
- Complete agenesis of the corpus callosum and trisomy 8
- Congenital chylothorax, a rare case of nonimmune fetal hydrops
- Congenital Diaphragmatic Hernia - a late onset of rare case
- Continuous antibiotic prophylaxis after birth and incidence of urinary tract infections in babies with antenatal hydronephrosis in the third trimester
- Cord cyst, the first sign of a polymalformative syndrom
- Correlation between cardiac function and brain development in fetuses with congenital diaphragmatic hernia (CDH)
- Cri-du-chat syndrome: a challenge of prenatal diagnosis
- Developmental changes of the coronary sinus between the first and second trimesters: a pilot study
- Diagnosis of fetal face anomalies
- Diagnostic performance of standardized first trimester fetal echocardiography for the detection of congenital heart defects
- Discrepancy in menstrual and ultrasound-based gestational age is associated with chromosomal aberrations and adverse pregnancy outcomes
- Early gestational development of ganglionic eminence: a comparative analysis between normal and aneuploid fetuses between 11 and 13+6 weeks
- Early prenatal diagnosis of semilobar holoprolencephaly
- Ebstein’s anomaly and tricuspid valve dysplasia - spectrum, associated anomalies and outcome after prenatal diagnosis
- Effects of maternal Mediterranean diet on fetal cardiac function. The IMPACT BCN trial
- Enlarged cavum septum pellucidum: diagnosis, implications and prognosis
- Epidemiological insights into anencephaly in a middle-income country: a comprehensive analysis of risk factors and social trends
- Feasibility and accuracy of the 'bat-sign' in the prenatal diagnosis of cleft palate
- Feasibility and limitations of the prenatal sonographic assessment of choanal flow
- Fetal abdominal tumors, a rare finding in obstetric ultrasound: multicentric experience in Chile
- Fetal arthrogryposis, vertebral anomalies and cystic hygroma - What now?
- Fetal ascites as the only finding of obstructive uropathy
- Fetal brain magnetic resonance imaging: comparing in-utero and postnatal imaging
- Fetal cardiac output measured by phase contrast magnetic resonance imaging using doppler ultrasound gating
- Fetal dilated jugular lymphatic sacs on first trimester ultrasound and their implications in antenatal screening
- Fetal ebstein anomaly and tricuspid dysplasia complicated by pulmonary insufficiency and circular shunt: therapeutic challenges and clinical outcome
- Fetal echocardiography indications: areas of consensus and controversy between guidelines and expert consensus
- Fetal hemodynamics in down syndrome and congenital heart disease
- Fetal hydronephrosis: diagnostic accuracy and neonatal outcomes in a tertiary care unit
- Fetal hydrops - mediastinal teratoma
- Fetal hydrops in the third trimester in a case with RASA1 mutation and Parkes-Weber syndrome
- Fetal intestinal volvulus: a prenatal diagnosis using two-dimensional and three-dimensional ultrasound
- Fetal intracranial haemorrhage: imaging findings and outcomes
- Fetal intracranial teratoma
- Fetal life marks the onset of biventricular restructuring in cases of tetralogy of fallot
- Fetal retroperitoneal masses – a diagnosis in the third trimester
- First trimester diagnosis of Cystic Hygromas: presentetion of fetal lymphangioma in association with chromosomal aberrations
- First trimester diagnosis of Prune Belly syndrome
- First-trimester biochemical markers in pregnancies with major fetal congenital heart defects: a cohort study
- Fraser Syndrome with Limb Reduction Defect: a rare and unique anatomic variation
- From the phenotype to the genotype: Apert syndrome
- Gastroschisis – prenatal diagnosis and neonatal follow-up, 3-year series in a Hospital in Southern Brazil
- High accuracy detection of transposition of the great arteries in 2nd trimester fetal ultrasound using artificial intelligence
- Ichthyosis fetalis - prenatal ultrasound and molecular diagnosis and postnatal course
- IMITAS: National implementation of first-trimester anomaly scan in The Netherlands
- Impact of early screening for congenital heart defects – a single-center study
- Interobserver reproducibility of ultrasound first trimester markers of SNC abnormalities
- Intestinal dilatation of the fetus: ultrasound diagnosis, management and neonatal prognosis: case report and literature review
- Intracardiac flow analysis of hypoplastic left heart syndrome neonates using a novel doppler velocity reconstruction (DoVeR)
- Isolated ventricular wall irregularities: incidental findings with a real impact on psychomotor development?
- Left pulmonary artery sling associated with a common atrioventricular canal defect and trisomy 21 – a rare diagnosis
- Limb malformations in the first trimester scan: a 14-year retrospective study
- Longitudinal assessment of abnormal cortical folding in fetuses and neonates with isolated non-severe ventriculomegaly
- Low PAPP-A (<0.3MoM) at first trimester screening and structural abnormalities in euploid fetuses
- Main cerebral fissures depth in fetuses affected by congenital heart disease
- Main cerebral fissures depth in fetuses affected by transposition of great arteries: impact of placental vascular malperfusion
- Management and outcomes in fetuses with gastroschisis: a 6-year review at a national referral center
- Maternal lipid levels in pregnancies with fetal congenital heart defects – a case-control study
- Missed anomalies on second trimester ultrasound in a low-risk population
- Mode of delivery and outcomes of fetuses with gastroschisis: a 6-year review
- Myelomeningocele and its possible ultrasound findings
- Nephronophthisis Type 2 – a novel variant associated with a prenatal form of ciliopathy
- Neurodevelopmental outcomes in fetuses with abdominal wall defects
- Non-severe ventriculomegaly: what to expect when you’re expecting
- Optimization of systematic neuroscreening of the fetal corpus callosum
- Osteogenesis imperfecta discovered in the third trimester
- Outcome of prenatally diagnosed idiopathic clubfoot: a retrospective observation study in a tertiary center between 2014 and 2023
- Outcome of vaginal delivery in fetuses with omphalocele
- Outcomes of a cohort of children with univentricular congenital heart diseases with and without prenatal diagnosis
- Partial hydatidiform mole in the second trimester
- Pathophysiology of absent leaflets of cavum septum pellucidum on prenatal ultrasound
- Pattern of major congenital anomalies in Brazil: a study from 2011 to 2020
- Perinatal thoraco-abdominal tumors management in infants: a multicenter experience
- Persistent right umbilical vein: obstetric surveillance and neonatal outcomes in a retrospective study
- Placenta percreta invading the urinary bladder
- Placental biochemical markers in pregnancies complicated by fetal congenital heart defects and in other pregnancies by the same mother – a case-control study
- Placental dysfunction in fetuses diagnosed with tetralogy of fallot: a prospective single-center cohort study at a tertiary hospital in barcelona
- Postnatal evaluation of prenatally detected hydronephrosis - results of a Swedish regional second trimester screening program 2019-2022
- Postnatal outcomes of prenatally detected ovarian fetal cysts: is surgery always the best choice?
- Postnatal outcomes of prenatally detected unilateral congenital renal anomalies: a single center experience
- Predicting cognitive and developmental disorders using deep learning
- Predicting the impact of low-density lipoprotein cholesterol lowering through different drug targets on risk of congenital heart disease
- Prediction of outcomes in uncomplicated moderate unilateral hydronephrosis – 3rd trimester scan vs. 1st postnatal scan
- Prenatal contralateral pulmonary artery diameter is the best prediction of the hernia size in congenital diaphragmatic hernia
- Prenatal detection and pregnancy outcome in pregnancies with fetal congenital heart defects – a nationwide study
- Prenatal detection of case of persistent fetal vasculature
- Prenatal detection of esophageal atresia: accuracy and limits
- Prenatal diagnosis of choledochal cyst
- Prenatal diagnosis of Coffin Siris Syndrome in a fetus with enlarged nuchal translucency who developed hypertrophic cardiomyopathy
- Prenatal diagnosis of congenital aortic arch anomaly: color doppler image as a supplement to image modality
- Prenatal diagnosis of generalized arterial calcification of infancy (GACI) in two Indian families
- Prenatal diagnosis of IVC interruption with azygos continuation
- Prenatal diagnosis of vermian cysts
- Prenatal differential diagnosis between Fanconi anemia and ART syndrome
- Prenatal prediction of vein of Galen malformation perinatal morbidity using ultrasound and super-resolution brain MRI
- Prenatal study of cavum septum pellucidum anomalies: our experience with 21 cases observed in the last five years
- Prenatal ultrasound diagnosis of right and double aortic arch
- Prenatal ultrasound findings of Hirschsprung's disease
- Prenatal ultrasound imaging in left-sided noncommunicating congenital diaphragmatic defects
- Prevalence and characteristics of fetal craniofacial anomalies in a 15-year timeline: insights from prenatal ultrasound evaluation
- Prevalence of outcomes in moderate fetal hydronephrosis based on additional features on the third trimester ultrasound scan
- Prospective diagnosis of facial clefts in the first trimester
- Recurrence of 3MC syndrome in four pregnancies in an Asian-Indian family: antenatal findings and molecular genetic studies
- Relationship between hindbrain herniation reversal and the need for hydrocephalus treatment in fetuses with prenatally repaired open spina bifida
- Report of births due to Congenital Anomalies in the most complex Pediatric Hospital of CABA, Argentina
- Results of 6 cases with ductus venosus agenesis in 7846 screened pregnancies. The role of exome sequencing
- Retrospective review of introduction of antenatal hypoplastic left heart pathway
- Severe infundibular pulmonary stenosis: prenatal diagnosis in the second trimester
- Severe ventriculomegaly: experience from a reference center
- Size of the fetal thymus according to the amniocentesis indication in the State Center for Timely Prenatal Screening in Mexico
- Sonographic features of placentation and intrauterine environment in pregnancy complicated by fetal arrhythmias
- Spectrum of prenatally detected callosal abnormalities in tribal region of eastern India – a multicentric study
- Spontaneous prenatal diagnosis of situs inversus totalis combined with complex congenital heart disease
- Stillbirth risk and congenital upper small bowel obstruction
- Successful pregnancy in a patient with Wolff-Parkinson-White syndrome
- Terminal meningomyelocele vs sacrococcygeal teratoma: searching a second opinion
- The carotic-subclavian artery index (CSAi) in the fetal aortic arch with classical branching and its variants in a low-risk population between 19 and 22 weeks of gestation
- The impact of first-trimester ultrasound on the early detection of fetal morphological anomalies (1994-2020)
- The predictive value of total fetal lung volume for respiratory distress syndrome and its relationship with betamethasone therapy
- The role of ai-assisted automated cardiac biometrics in screening for fetal coarctation of the aorta
- The role of third trimester ultrasound and central nervous system evaluation: a septo-optic dysplasia clinical case
- The true nature of the small branches: an in depth look at the early second trimester pericallosal arteries in normal and pathologic conditions
- Timely Diagnosis and Management of Neonatal Duodenal Atresia
- Understanding prognosis and management of nasal bone anomalies detected prenatally: insights from a study of thirteen cases
- Unraveling the enigma: congenital midgut volvulus - exploring rare bowel dilation in late gestation
- Unveiling the mysteries: exploring a case of Scimitar syndrome
- Visualisation of the fetal corpus callosum in routine second trimester screening ultrasound examinations
- When posterior urethral valves are suspected on third trimester – what to expect?
- Аgenesis of the ductus venosus, varicose veins of the umbilical cord, persistent superior vena cava