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

