Malformations.org

Here is the list of developmental anomalies associated with this developmental anomaly, based on the cases' information :

• Polysplenia 6.38% (3/47 anomalies), in cases MDB5, MDB189, MDB516
• Intestinal malrotation 4.26% (2/47 anomalies), in cases MDB5, MDB516
• Pulmonary hypoplasia 4.26% (2/47 anomalies), in cases MDB189, MDB516
• Facial dysmorphism 2.13% (1/47 anomalies), in case MDB5
• Flat face 2.13% (1/47 anomalies), in case MDB5
• Flattened occiput 2.13% (1/47 anomalies), in case MDB5
• Epicanthus 2.13% (1/47 anomalies), in case MDB5
• Macroglossia 2.13% (1/47 anomalies), in case MDB5
• Transverse palmar crease, bilateral 2.13% (1/47 anomalies), in case MDB5
• Atrial Hypertrophy 2.13% (1/47 anomalies), in case MDB5
• Overlapping toes 2.13% (1/47 anomalies), in case MDB5
• Preauricular hamartoma 2.13% (1/47 anomalies), in case MDB5
• Ventricular septal defect, membranous 2.13% (1/47 anomalies), in case MDB5
• Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 2.13% (1/47 anomalies), in case MDB5
• Dilatation of ureter , bilateral, congenital 2.13% (1/47 anomalies), in case MDB5
• Fusion of the adrenal glands 2.13% (1/47 anomalies), in case MDB5
• Cystic hygroma 2.13% (1/47 anomalies), in case MDB5
• Lung agenesis, unilateral 2.13% (1/47 anomalies), in case MDB5
• Talipes equinovarus, bilateral 2.13% (1/47 anomalies), in case MDB5
• Unilobate lung, unilateral 2.13% (1/47 anomalies), in case MDB5
• Bladder wall thickness 2.13% (1/47 anomalies), in case MDB5
• Amnion nodosum 2.13% (1/47 anomalies), in case MDB5
• Left pulmonary isomerism 2.13% (1/47 anomalies), in case MDB189
• Persistent left superior vena cava 2.13% (1/47 anomalies), in case MDB189
• Common atrium 2.13% (1/47 anomalies), in case MDB189
• Atrioventricular - channel 2.13% (1/47 anomalies), in case MDB189
• Defective developement of left ventricle 2.13% (1/47 anomalies), in case MDB189
• Interventricular septal thickness 2.13% (1/47 anomalies), in case MDB189
• Transverse aortic hypoplasia 2.13% (1/47 anomalies), in case MDB189
• Hypoplasia of ascending aorta 2.13% (1/47 anomalies), in case MDB189
• Left atrial isomerism 2.13% (1/47 anomalies), in case MDB189
• Renal hypoplasia 2.13% (1/47 anomalies), in case MDB189
• Adrenal hypoplasia, fetal 2.13% (1/47 anomalies), in case MDB189
• Nonimmune hydrops fetalis (NIHF) 2.13% (1/47 anomalies), in case MDB516
• Ascites, fetal 2.13% (1/47 anomalies), in case MDB516
• Left-Sidedness, bilateral 2.13% (1/47 anomalies), in case MDB516
• Trilobate lung, left 2.13% (1/47 anomalies), in case MDB516
• Hepatomegaly, fetal 2.13% (1/47 anomalies), in case MDB516
• Placental hydrops 2.13% (1/47 anomalies), in case MDB516
• Hypogenesis of the Cerebellar Vermis 2.13% (1/47 anomalies), in case MDB516
• Single cerebral ventricule 2.13% (1/47 anomalies), in case MDB516
• Corpus callosum agenesis 2.13% (1/47 anomalies), in case MDB516
• Absence of the Septum Pellucidum 2.13% (1/47 anomalies), in case MDB516