Defects
- A case of a giant chorioangioma
- A case of a giant chorioangioma
- A case of a variant Turner syndrome phenotype
- A case of achondrogenesis Type 2
- A case of acute myocardial infarct complicating pregnancy
- A case of amniotic band syndrome
- A case of amniotic band syndrome
- A case of anomalous venous return
- A case of aortic dissection in a pregnant patient with Marfan syndrome
- A case of auriculo-condylar syndrome
- A case of caudal regression syndrome
- A case of chorioangioma
- A case of Cri du Chat syndrome
- A case of Crouzon Syndrome
- A case of cystic hygroma
- A case of Diastrophic Dysplasia
- A case of encephalocele
- A case of familial Van der Woude syndrome and Popliteal Pterygium syndrome
- A case of forearm tumor
- A case of frontal and parietal cephalocele
- A case of herlequin fetus, ichthyosis congenita
- A case of heterotaxy syndrome
- A case of I Cell disease
- A case of large cystic hygroma
- A case of late gestational idiopathic constriction of fetal ductus arteriosus
- A case of left congenital diaphragmatic hernia
- A case of left isomerism
- A case of lobar holoprosencephaly with mega cisterna magna
- A case of malposition of the great arteries with intraventricular septal defect
- A case of megacystis
- A case of multiple pterygium syndrome
- A case of neonatal genital prolapse
- A case of pentalogy of Cantrell
- A case of persistent right umblical vein
- A case of phocomelia associated with diaphragmatic hernia
- A case of prenatal diagnosis of bilateral schizencephaly
- A case of primitive neuroectodermal brain tumor
- A case of proximal focal femoral hypoplasia
- A case of pseudoaminopterin syndrome
- A case of recurrent Bartter syndrome
- A case of supracardiac total anomalous pulmonary venous return
- A case of ventriculo-coronary arterial communication in pulmonary atresia with intact ventricular septum
- A case of Waardenburg syndrome
- A case of Zellweger Syndrome
- A new semi-automated method for measuring volume of structures in the fetal brain
- A previously unreported association between Noonan and related syndromes and anomalous left brachiocephalic vein
- A rare gastrointestinal cause of non-immune hydrops fetalis: Meconium plug syndrome
- A watertight fetal repair reverses hindbrain herniation and improves neuromotor function in spina bifida lamb model
- Absent pulmonary valve: a prenatal case series
- Accuracy of early fetal echocardiography in the diagnosis of outflow tracts anomalies in a high-risk population
- Anomalies of the aortic arch: correlation between prenatal ultrasonography and postnatal MRI/CT
- Anomalous origin of a Shepherd Hook ductus arteriosus: an obstructive kink should be of concern
- Antenatal predictors of neonatal outcome in prenatally diagnosed isolated left-sided congenital diaphragmatic hernia
- Antepartum transabdominal amnioinfusion in idiopathic oligohydramnios
- Assessment of the fetal kidneys during the first trimester scan
- Assessment of the presence of 'Maxillary gap' in the first trimester scan
- Association between 1p36 copy number variations, abnormal expression of PEX10 gene and epilepsy phenotype
- Cardiac axis and V sign angle: potential markers of congenital heart defects in the first trimester
- Cerebellar Doppler velocimetry in fetal rats with spina bifida
- Cerebral damage in congenital heart defects. Do they exist before we thought?
- Combined double chambered right ventricle and discrete subaortic stenosis
- Comparison of fetal echocardiography with fetal cardiac MRI in the human fetus
- Congenital heart defects in fetuses exposed to antidepressants during the first trimester of pregnancy
- Connatal cyst : Antenatal findings and differential diagnoses
- Contemporary management of fetal anemia due to red cell alloimmunisation: factors affecting perinatal outcome
- Corrected transposition of the great arteries with mild discrete subpulmonary stenosis
- Deafness genetic testing and prenatal diagnosis analysis of fourteen families
- Detection of structural abnormalities in the first trimester using a specific examination protocol
- Diagnostic algorithm and protocol for the management of fetal ascites
- Difficulties of fetal echocardiography: coarctation of the fetal aorta
- Discrepancy in fetal head biometry between ultrasound and MRI in suspected microcephalic fetuses
- Dynamical model based simulator of fetal cardiotocography for educational training purposes
- Effectiveness of fetal heart examination at the 20-24 weeks scan
- Effects of abdominal decompression on fetal umbilical artery and middle cerebral artery blood flow
- Estimation of the detection rate of cardiac defects in the first trimester after including the outflow tract views.
- Feasibility study to detect abnormal rhythmic elements in fetal congenital heart disease using fetal electrocardiography
- Fetal abnormalities associated with single umbilical artery and genetic counselling
- Fetal bowel dilatation from diagnosis to treatment
- Fetal Brain Anomalies Detection during the First Trimester: Expanding the Scope of Antenatal Sonography.
- Fetal isolated hydrocephalus associated with a novel missense mutation of L1CAM
- Fetal mild ventriculomegaly: the correlation between the degree of dilatation and other fetal biometric parameters
- Fetal MRI to assess fetal airway obstruction
- First trimester diagnosis of cystic hygroma by transvaginal ultrasound and cytogenetic evaluation
- First trimester diagnosis of frontonasal dysplasia
- First Trimester Megacystis Due to Obstructive Uropathy
- Functional ultrasound evaluation of the fetal heart at 11-14 weeks of pregnancy in increased NT fetuses
- Gastro-cardiac angle - A novel method to predict liver herniation in left congenital diaphragmatic hernia
- Genetic diagnosis of severe fetal akinesia syndrome by means of whole exome sequencing
- Hydrops fetalis with deletion of macro domain containing 2
- Hypoplasia or aplasia of the vermis in fetuses with crown-rump length between 45 and 84 mm
- Immunomodulatory effects of umbilical cord-derived mesenchymal stem cells
- Incidence of congenital heart defects in IVF/ICSI pregnancy: a systematic review and meta-analysis
- Learning curve for ultrasound assessment of the fetal heart in nuchal scan
- Limited Dorsal Myeloschisis: a diagnostic pitfall in the prenatal ultrasound of fetal dysraphism
- Magnetic resonance imagingT1 relaxation properties of fetal blood in normal fetuses and fetuses suspected of anemia
- Maxillary gap sign at 11-13 weeks – intra- and interobserver reliability in isolated cases of cleft lip and palate
- Microarray-based analysis in prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with CHD
- Molecular cytogenic investigation in fetus with ventriculomegaly
- Molecular genetic analysis of 3 patients featuring mental retardation and developmental delay
- Natural history of isolated fetal ventriculomegaly: agreement between pre- and postnatal imaging
- Neuro-developmental outcome of children with a measurement of nuchal translucency > 95th centile in first trimester
- Neurodevelopmental outcome of isolated ventriculomegaly: a prospective cohort study
- Nonimmune Hydrops Fetalis: Ultrasound diagnosis in patients with systemic autoimmune diseases
- Obstetric outcome of pregnancies complicated by anencephaly: a 25 year single hospital experience
- Outcome and chromosomal abnormalities in fetuses with isolated persistent left superior vena cava
- Outcomes of neonates with prenatally diagnosed congenital heart disease
- Perinatal predictors for respiratory and gastrointestinal outcomes in children managed with isolated CDH
- Placental chorioangioma and fetal hepatic hemangioma coexistence causing fetal high-output heart failure
- Placental epigenetic biomarkers for the detection of isolated ventricular septal defect
- Pregnancy outcome of fetuses with increased nuchaltranslucency but normal karyotype and CMA
- Premature closure of the cranial sutures - the new de novo mutation
- Prenatal diagnosis of coarctation of the aorta in a fetus with asplenia and right atrial isomerism
- Prenatal diagnosis of Dandy-Walker malformation
- Prenatal diagnosis of duplication cyst of the tongue
- Prenatal diagnosis of ebstein anomaly – from normal to severe disease
- Prenatal diagnosis of esophageal atresia: a prospective study
- Prenatal diagnosis of foetal hepatic vascular anomalies : case reports and review of the literature
- Prenatal diagnosis of hydranencephaly
- Prenatal diagnosis of primary immunodeficiency: an emerging experience in Egypt
- Prenatal diagnosis of sacrococcygeal teratoma
- Prenatal diagnosis of split hand/foot malformation
- Prenatal evaluation of fetal interrupted aortic arch type A
- Prenatal features of neurofibromatosis type 1
- Prospective validation of a prenatal score for prediction of postnatal outcome in cases with critical pulmonary stenosis
- Recurrent microlissencephaly: a case report
- Recurrent pregnancy loss due to hydrops fetalis caused by alpha thalassemia
- Right aortic arch with vascular ring and aberrant left subclavian artery
- Role of 3D imiging in the prediction of prognosis for mega-urethra
- Short term variation of the fetal heart rate: normal values for 2 different computational algorithms
- Short-rib polydactyly syndrome: antenatal diagnosis
- Simplified diagnosis of heterotaxy
- SNP array to identify pathogenic copy number variations in fetuses with defects and women with adverse reproductive history
- Sonographic detection of fetal gallbladder duplication
- STIC recorded hemodynamics in D transposition of the great arteries with VSD
- Stomach in contact with the bladder in left congenital diaphragmatic hernia
- Targeted sequencing of maternal plasma for haplotype-based noninvasive prenatal testing of spinal muscular atrophy
- Technical aspects of fetal cardiac interventions - 6 years experience at one center
- The added yield of whole exome sequencing in fetuses with suspected central nervous system abnormalities
- The outcome of isolated prenatal ventricular size disproportion in the absence of aortic coarctation
- Ultrasound marker for detecting isolated congenital heart diseases in the first trimester
- Van der Woude syndrome family tree