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

• Facial dysmorphism 6.06% (6/99 anomalies), in cases MDB238, MDB332, MDB452, MDB481, MDB168, MDB257
• Low-set ears 5.05% (5/99 anomalies), in cases MDB238, MDB249, MDB332, MDB168, MDB257
• Intrauterine growth retardation, symmetric 5.05% (5/99 anomalies), in cases MDB249, MDB332, MDB452, MDB481, MDB168
• Hypertelorism 3.03% (3/99 anomalies), in cases MDB238, MDB481, MDB257
• Placenta hypoplasia 3.03% (3/99 anomalies), in cases MDB249, MDB332, MDB452
• Retrognathia 3.03% (3/99 anomalies), in cases MDB332, MDB481, MDB168
• Nonimmune hydrops fetalis (NIHF) 3.03% (3/99 anomalies), in cases MDB481, MDB168, MDB257
• Corpus callosum agenesis 2.02% (2/99 anomalies), in cases MDB8, MDB481
• Micrognathia 2.02% (2/99 anomalies), in cases MDB238, MDB257
• Arthrogryposis 2.02% (2/99 anomalies), in cases MDB238, MDB257
• Pulmonary hypoplasia 2.02% (2/99 anomalies), in cases MDB238, MDB168
• Talipes equinovarus, bilateral 2.02% (2/99 anomalies), in cases MDB238, MDB257
• Triangular face 2.02% (2/99 anomalies), in cases MDB332, MDB452
• Lobulated, fused and horseshoe kidney 2.02% (2/99 anomalies), in cases MDB332, MDB257
• Ventricular septal defect, muscular 2.02% (2/99 anomalies), in cases MDB452, MDB257
• Adrenal hypoplasia, fetal 2.02% (2/99 anomalies), in cases MDB452, MDB168
• Clindodactyly of 5th finger, bilateral 2.02% (2/99 anomalies), in cases MDB481, MDB168
• Cystic hygroma 2.02% (2/99 anomalies), in cases MDB168, MDB257
• Neck edema 1.01% (1/99 anomalies), in case MDB8
• Pectus excavatum 1.01% (1/99 anomalies), in case MDB8
• Syndactyly, simple (webbed), fingers 1.01% (1/99 anomalies), in case MDB238
• Overlapping fingers 1.01% (1/99 anomalies), in case MDB238
• Scoliosis, congenital 1.01% (1/99 anomalies), in case MDB238
• Axillary pterygia, bilateral 1.01% (1/99 anomalies), in case MDB238
• Renal hypertropy, fetal, bilateral 1.01% (1/99 anomalies), in case MDB238
• Omphalocele 1.01% (1/99 anomalies), in case MDB249
• Polydactyly of the hand, preaxial 1.01% (1/99 anomalies), in case MDB249
• Syndactyly of the fingers, complex, unilateral 1.01% (1/99 anomalies), in case MDB249
• Arthrogryposis,lower limbs 1.01% (1/99 anomalies), in case MDB249
• Triploidy, Maternal, nonmolar (triploidy by digyny) 1.01% (1/99 anomalies), in case MDB332
• Prominent and pointed nose 1.01% (1/99 anomalies), in case MDB332
• Syndactyly of the fingers, complex, bilateral 1.01% (1/99 anomalies), in case MDB332
• Syndactyly of the toes, complex, bilateral 1.01% (1/99 anomalies), in case MDB332
• Aortic valve atresia 1.01% (1/99 anomalies), in case MDB332
• Pulmonary artery dilatation, fetal 1.01% (1/99 anomalies), in case MDB332
• Placental hypermaturity 1.01% (1/99 anomalies), in case MDB332
• Cleft lip, unilateral 1.01% (1/99 anomalies), in case MDB452
• Persistent truncus arteriosus 1.01% (1/99 anomalies), in case MDB452
• Ambiguous genitalia 1.01% (1/99 anomalies), in case MDB481
• Posteriorly inclined and low-positioned ears 1.01% (1/99 anomalies), in case MDB481
• Dolicocephaly 1.01% (1/99 anomalies), in case MDB481
• Transverse palmar crease, bilateral 1.01% (1/99 anomalies), in case MDB481
• Imperforate Anus 1.01% (1/99 anomalies), in case MDB481
• Rocker-bottom feet 1.01% (1/99 anomalies), in case MDB481
• Persistent left superior vena cava 1.01% (1/99 anomalies), in case MDB481
• Pulmonary artery hypoplasia 1.01% (1/99 anomalies), in case MDB481
• Dextroposition of aorta 1.01% (1/99 anomalies), in case MDB481
• Renal hypoplasia, unilateral 1.01% (1/99 anomalies), in case MDB481
• Renal agenesis, unilateral 1.01% (1/99 anomalies), in case MDB481
• Ureteral duplication, complete, unilateral 1.01% (1/99 anomalies), in case MDB481
• Thymic hypoplasia 1.01% (1/99 anomalies), in case MDB481
• Presence of an infantile uterus with both testes 1.01% (1/99 anomalies), in case MDB481
• Absence of the Septum Pellucidum 1.01% (1/99 anomalies), in case MDB481
• Probst bundle 1.01% (1/99 anomalies), in case MDB481
• Cerebral ventriculomegaly 1.01% (1/99 anomalies), in case MDB481
• Hypoplasia of the liver 1.01% (1/99 anomalies), in case MDB168
• Hexadactyly, postaxial 1.01% (1/99 anomalies), in case MDB168
• Dysplasia of deep nuclei (olive dysplasia) 1.01% (1/99 anomalies), in case MDB257
• Hydrocephalus, Non-communicating 1.01% (1/99 anomalies), in case MDB257
• Microphthalmia 1.01% (1/99 anomalies), in case MDB257
• Frontal bossing 1.01% (1/99 anomalies), in case MDB257
• Small mouth 1.01% (1/99 anomalies), in case MDB257
• Long philtrum 1.01% (1/99 anomalies), in case MDB257
• Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 1.01% (1/99 anomalies), in case MDB257
• Hypogenesis of pyramidal tracts 1.01% (1/99 anomalies), in case MDB257
• Stenosis of aqueduct of Sylvius 1.01% (1/99 anomalies), in case MDB257
• Unilobate lung, bilateral 1.01% (1/99 anomalies), in case MDB257