Defects
- 3D/4D fetal echocardiography using spatio-temporal image correlation technology
- A case of 22q11. 2 duplication in a fetus with increased nuchal translucency and left-sided pleural effusion
- A case of absence of ductus venosus in right atrial isomerism
- A case of amniotic band syndrome
- A case of autosomal dominant inherited Diamond-Blackfan Anemia
- A case of bladder exstrophy
- A case of CCAM
- A case of cloacal extrophy
- A case of common arterial trunk with right aortic arch
- A case of complete atrioventricular block with complication of postnatal sepsis
- A case of congenital atrio ventricular block AVB in pregnancy
- A case of cystic fibrosis presenting as a distended bowel in third trimester
- A case of duodenal atresia
- A case of dural sinus malformation
- A case of ectopia cordis at the 11 to 14 weeks scan
- A case of facial teratoma
- A case of fetal goiter and profound hypothyroidism due to treatment of Grave’s disease
- A case of fetal liver tumor diagnosed prenatally
- A case of gastrointestinal duplication
- A case of Goldenhar syndrome
- A case of Harlequin ischthyosis
- A case of holoprosencephaly
- A case of holoprosencephaly and dandy walker malformation associated with triploidy
- A case of Kasabach-Merritt syndrome
- A case of lymphangioma of the fetal face
- A case of Meckel-Gruber syndrome
- A case of microcephaly
- A case of Mucopolysaccharidosis type VII (Sly Syndrome)
- A case of ovarian goitre
- A case of Pallister-Killian Syndrome in the first trimester
- A case of Pierre Robin sequence
- A case of prenatal diagnosis of osteogenesis imperfecta type II
- A case of prenatal pulmonary emphysema
- A case of prenatal ultrasound diagnosis of hypoplastic left heart syndrome
- A case of rare bosma arhinia microphthalmia syndrome
- A case of recurrent intracranial fetal hemorrhage, not associated with prematurity
- A case of right isomerism
- A case of sacrococcygeal teratoma
- A case of simple renal cyst
- A case of sirenomelia - Mermaid syndrome
- A case of Smith-Lemli-Opitz syndrome
- A case of tetra-phocomelia
- A case of twin pregnancy with tetralogy of Fallot and lobar holoprosencephaly
- A case of ureteropelvic junction obstruction with contralateral dysplastic kidney
- A case of VACTERL Association
- A case of Vein of Galen aneurysm
- A case of venous malformation of Galen diagnosis
- A retrospective review of sonographic markers for detection of open spina bifida at 11-14 weeks
- Abnormal cavum septi pellucidi: beyond corpus callosum agenesis
- Added clinical value of fetal brain magnetic resonance after a systematic neurosonography in congenital heart defects
- Agenesis of ductus venosus
- Agreement between prenatal and postnatal diagnosis of cardiovascular abnormalities
- Antenatal diagnosis and management of fetal midgut volvulus
- Antenatal diagnosis of persistent right umbilical Vein: Incidence and frequence of associated congenital malformations
- Antenatal ultrasonographic diagnosis of diastematomyelia
- Anterior abdominal wall defects: correlation between antenatal findings and postnatal outcome
- Apparent diffusion coefficient levels in fetuses with brain magnetic resonance T2 Hyper-intense signal
- Assessment of the corpus callosum in fetuses with isolated non-severe ventriculomegaly
- Bowel obstruction presented with reduced fetal movements
- Cardiac axis in the first trimester of gestation
- Cardiac axis in the screening of congenital heart defects in the first trimester
- Cardiac axis measurement in the first-trimester screening ultrasound
- Characterization of the congenital heart disease prenatally diagnosed
- Comparing the results of ultrasound findings to fetal autopsies: a retrospective study in a tertiary center
- Comparison of isolated versus multiple fetal liver calcifications long term prognosis
- Congenital malformations of the abdominal wall: omphalocele and laparoschisis
- Cortical development in fetuses with isolated non-severe ventriculomegaly and neurodevelopmental performance
- Detection of congenital heart defects in the first trimester using measurements of NT and DV in euploid fetuses
- Diagnosis of fetal ovarian torsion presenting with fetal abdominal solid mass and ascites
- Diagnosis of fetal structural abnormalities using whole exome sequencing
- Differential effect in corpus callosum development in fetuses with Congenital Heart Defect assessed by ultrasound
- Distended jugular lymphatic sacs in the first trimester of pregnancy
- Distribution of ventricular volumes in fetuses with isolated non-severe ventriculomegaly and neurodevelopmental outcome
- Ductus venosus agenesis as a marker of Pallister-Killian syndrome
- Dynamic fetal cardiac MRI using Doppler ultrasound gating in the assessment of the fetal aortic arch
- Early diagnosis of fetal brain migration abnormality
- Early fetal echocardiography: indications, abnormal findings and comparison with postnatal results
- Early nutrition in children with critical congenital heart defects and long-term growth
- Early prenatal diagnosis of osteogenesis imperfecta by 2D and 3D ultrasound
- Early prophylaxis of multiple micro-abnormalities in the development of the nervous system in the fetus
- Early spontaneous resolution of meconium peritonitis
- Effectiveness of prenatal ultrasound examination at the second trimester in detecting congenital abnormalities
- Esophageal atresia: prenatal detection rates in multiple versus singleton pregnancies
- Evaluation of the performance of the fetal heart morphological screening test
- Fetal and maternal outcomes in pregnancies complicated by congenital heart defects
- Fetal brain anomalies detection during the first trimester: expanding the scope of antenatal sonography
- Fetal brain examination: anterior-posterior complexes and landmarks of the proximal hemisphere
- Fetal brain MRI in polyhydramnios: Is it justified?
- Fetal brain ultrasonography and MRI of the corpus callosum and transverse cerebellar diameter
- Fetal exposure to magnetic resonance imaging and neuro-developmental outcome
- Fetal hydrothorax with spontaneous resolution
- Fetal intraabdominal umbilical vein varix complicated with intrauterine fetal death
- Fetal intracranial calcifications, not just congenital TORCH infection
- Fetal occipital encephalocele: Case Series
- First trimester fetal heart assessment: influence of maternal body mass index and ultrasound approach
- Five step approach for screening and diagnosis for fetal heart defects in prenatal ultrasound
- Generalised arterial calcification of infancy
- Giant isolated exomphalos: role of prenatal diagnosis in prognosis and after birth treatment coordination
- Helping mothers to better understand their child’s fetal cardiac anomaly with 3D printing
- Interleukin 10 receptor gene mutations in very early–onset inflammatory bowel disease: presentation of two cases
- Is persistent left superior vena cava a benign finding in fetus? Analysis of 27 cases from a fetal cardiology centre
- Isolated versus associated pathology of fetal abdominal cystic masses in the second and third trimesters of pregnancy
- Knowledge of antenatal patients on fetal anomaly screening in Northern Nigeria
- Longitudinal changes of cardiovascular parameters in fetuses with congenital atrioventricular block
- Management of rare cases of fetal abdominal cystic lesions
- Mediastinal shift angles by ultrasound and MRI in isolated left sided congenital diaphragmatic hernia
- Micrognathia and associated anomalies, aneuploidies and genetic syndromes
- Natural history of fetal isolated ventriculomegaly: Comparison between pre- and post-natal imaging
- Neurodevelopmental outcome following prenatal diagnosis of a short corpus callosum
- Neurodevelopmental outcome of fetal intracranial haemorrhage: MRI-Based Cohort Study
- Neurodevelopmental outcome of fetal isolated ventricular asymmetry without dilation
- Outcome of prenatally diagnosed Cavum velum Interpositum cyst
- Patterns of cortical development assessed by neurosonography in PE with or without FGR
- Persistent left superior vena cava without associated congenital heart defect
- Personalized charts for fetal corpus callosum length: rationale and clinical application
- Polyhydramnios: associated conditions with this ultrasound finding and pregnancy outcomes
- Prediction of facial features of fetal alcohol syndrome at 1 year of age by surface rendered images of the face at 28-31 weeks
- Prenatal and neonatal outcome of hyperechogenic bowel: report on 184 prenatal cases
- Prenatal detection of congenital abnormalities
- Prenatal detection of esophageal atresia: comparing a standard level two vs a tertiary center expert anomaly scan
- Prenatal diagnois of isolated massive liver calcifications with spontaneous resolution in the neonatal period
- Prenatal diagnosis and outcome of subcutaneous occipital cysts
- Prenatal diagnosis of a gastric duplication cyst: utility of magnetic resonance imaging
- Prenatal diagnosis of an arachnoid cyst in the posterior fossa
- Prenatal diagnosis of arachnoid cysts: MRI features and neurodevelopmental outcome
- Prenatal diagnosis of carnitine palmitoyl transferase II deficiency
- Prenatal diagnosis of congenital face and neck malformations- is complementary fetal MRI of value?
- Prenatal diagnosis of facial clefts and associated anomalies
- Prenatal diagnosis of FGF20 gene mutation associated with recurrent bilateral renal agenesis
- Prenatal diagnosis of Scimitar syndrome: a series of six cases
- Prenatal diagnosis of two cases of pentalogy of Cantrell that show the broad spectrum of the syndrome
- Prenatal features and outcome of fetal aneurysms and diverticula
- Prenatal findings of aortico-left ventricular tunnel: the good and the ugly
- Prenatal regression of cerebral ventriculomegaly: a three case series
- Prenatal series of first trimester cardiac anomalies with sonopathological correlation: Series of 100 cases: Lessons learnt
- Prenatal sonographic diagnosis of Right Isomerism associated with Sliding Hiatal hernia
- Prenatal ultrasound detection of fetal axillary lymphangioma and long term follow up
- Prenatal USG presentation, diagnosis and outcome of fetal echogenic lung lesions
- Prenatally detected case of CCAM type 1 associated with deficiency of alpha 1 antitrypsin
- Prenatally diagnosed cardiac rhabdomyomas: characteristics and outcome
- Prevalence and factors associated with congenital malformations in fetal stillbirth
- Prognostic predictive value of diffusion-weighted magnetic resonance imaging of the brain in small for gestational age fetuses
- Prospective detection and differential diagnosis of cystic posterior fossa anomalies by assessing posterior brain at 11-14 weeks
- Report on a prenatal Dandy-Walker malformation recurrence
- Retrospective review of the management of antenatally detected ovarian lesions at a tertiary-level paediatric surgery unit
- Rhomboencephalosynapsis - prenatal diagnosis and outcome
- Right ventricular outflow tract anomalies in monochorionic twin pregnancies diagnosed prenatally
- Risk of preeclampsia, small for gestational age and placental abnormalities in pregnancies with major congenital heart disease
- Risk of spontaneous and iatrogenic preterm birth in pregnancies with prenatal diagnosis of major congenital heart disease
- Routine examination of fetal posterior fossa in transverse section at 11 – 14 weeks
- Sequential axial approach for the routine ultrasound evaluation of basic fetal anatomy at 11-13 weeks
- Simulations predict ductus venosus angle of insertion affects qualitative and quantitative flow across the foramen ovale
- Six years´ experience with prenatally diagnosed left congenital diaphragmatic hernia
- Smith-Magenis syndrome after ultrasonographic detection of semilobar holoprosencephaly at 12 weeks
- Syndrome of caudal regression in the fetus of a diabetic mother
- Tetralogy of Fallot and malalignment ventricular septal defect detected at early echocardiography
- Thanatophoric dwarfism: a lethal osteochondrodysplasias
- The achievement of pregnancy with eisenmenger syndrome
- The contribution of ultrasound in the antenatal diagnosis of omphalocele and gastroschisis
- The normal development of the cave of septum pellucidum - A fetal MRI study
- The role of fetal MRI for evaluating brain pathology in fetuses with abnormal chromosomal microarray analysis
- The role of karyotype investigation in a case of antenatal diagnosis of club feet
- The variable ultrasound features in the semilobar form of holoprocencephaly
- The very early anomaly scan from screening chromosomal defects to early detection of congenital anomalies
- Transverse cerebellar diameter: alternative parameter for gestational age assessment in Northern Nigeria
- Trends in termination of pregnancy for neural tube defects in England and Wales
- Tricuspid regurgitation and adverse fetal outcome
- Two cases of body stalk complex
- Two dimensional visualisation of optic chiasma
- Two-year follow up of children with prenatally diagnosed univentricular heart
- Ultrasound prenatal diagnosis and subsequent management of a fetus in fetus case
- Unilateral multicystic renal dysplasia – complete prenatal involution
- Usefulness of magnetic resonance imaging for prenatal management of ventriculomegaly
- Van der Woude syndrome family tree