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• () in case MDB

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

• Dilatation of ureter , bilateral, congenital 4.49% (8/178 anomalies), in cases MDB320, MDB324, MDB388, MDB439, MDB462, MDB500, MDB519, MDB23
• Hypertelorism 3.93% (7/178 anomalies), in cases MDB198, MDB320, MDB336, MDB346, MDB372, MDB394, MDB439
• Facial dysmorphism 2.81% (5/178 anomalies), in cases MDB198, MDB320, MDB346, MDB394, MDB439
• Hydronephrosis, congenital, bilateral 2.81% (5/178 anomalies), in cases MDB320, MDB489, MDB500, MDB23, MDB76
• Megacystis 2.25% (4/178 anomalies), in cases MDB320, MDB324, MDB500, MDB519
• Micrognathia 2.25% (4/178 anomalies), in cases MDB320, MDB324, MDB489, MDB500
• Pulmonary hypoplasia 2.25% (4/178 anomalies), in cases MDB324, MDB372, MDB388, MDB23
• Broad nasal bridge 1.69% (3/178 anomalies), in cases MDB198, MDB320, MDB439
• Lobulated, fused and horseshoe kidney 1.69% (3/178 anomalies), in cases MDB320, MDB439, MDB462
• Flattened nose 1.69% (3/178 anomalies), in cases MDB320, MDB324, MDB500
• Hepatomegaly, fetal 1.69% (3/178 anomalies), in cases MDB336, MDB351, MDB519
• Hypospadias, penile 1.69% (3/178 anomalies), in cases MDB372, MDB394, MDB462
• Sloping forehead 1.12% (2/178 anomalies), in cases MDB198, MDB324
• Low-set ears 1.12% (2/178 anomalies), in cases MDB198, MDB489
• Neck edema 1.12% (2/178 anomalies), in cases MDB198, MDB324
• Posterior urethral valves, congenital 1.12% (2/178 anomalies), in cases MDB320, MDB500
• Multicystic renal dysplasia,bilateral 1.12% (2/178 anomalies), in cases MDB320, MDB23
• Bladder wall thickness 1.12% (2/178 anomalies), in cases MDB320, MDB462
• Long philtrum 1.12% (2/178 anomalies), in cases MDB320, MDB324
• Posteriorly inclined and low-positioned ears 1.12% (2/178 anomalies), in cases MDB320, MDB324
• Thin upper lip 1.12% (2/178 anomalies), in cases MDB320, MDB346
• Gothic palate 1.12% (2/178 anomalies), in cases MDB320, MDB372
• Potter deformity sequence 1.12% (2/178 anomalies), in cases MDB324, MDB500
• Potter's facies 1.12% (2/178 anomalies), in cases MDB324, MDB500
• Clindodactyly of 5th finger, bilateral 1.12% (2/178 anomalies), in cases MDB324, MDB23
• Nonimmune hydrops fetalis (NIHF) 1.12% (2/178 anomalies), in cases MDB336, MDB76
• Dysplasia of deep nuclei (olive dysplasia) 1.12% (2/178 anomalies), in cases MDB336, MDB351
• Microcephaly 1.12% (2/178 anomalies), in cases MDB336, MDB351
• Corpus callosum agenesis 1.12% (2/178 anomalies), in cases MDB351, MDB394
• Coarctation of aorta, 1.12% (2/178 anomalies), in cases MDB372, MDB489
• Intrauterine growth retardation, symmetric 1.12% (2/178 anomalies), in cases MDB388, MDB489
• Bladder dilatation, fetal 1.12% (2/178 anomalies), in cases MDB394, MDB462
• Imperforate Anus 1.12% (2/178 anomalies), in cases MDB439, MDB462
• Megarectum 1.12% (2/178 anomalies), in cases MDB439, MDB462
• Short philtrum 0.56% (1/178 anomalies), in case MDB198
• Cerebral ventriculomegaly 0.56% (1/178 anomalies), in case MDB204
• Auricular dilatation 0.56% (1/178 anomalies), in case MDB204
• Badly-hemmed ears 0.56% (1/178 anomalies), in case MDB320
• Microstomia 0.56% (1/178 anomalies), in case MDB320
• Cleft palate, median posterior 0.56% (1/178 anomalies), in case MDB320
• Short neck 0.56% (1/178 anomalies), in case MDB320
• Placenta hypoplasia 0.56% (1/178 anomalies), in case MDB320
• Hypospadias, Glandular 0.56% (1/178 anomalies), in case MDB320
• Hypoplasia and dysplasia of the kidney, bilateral 0.56% (1/178 anomalies), in case MDB324
• Low nasal bridge 0.56% (1/178 anomalies), in case MDB324
• Talipes equinovarus, bilateral 0.56% (1/178 anomalies), in case MDB324
• Pericardial effusion 0.56% (1/178 anomalies), in case MDB324
• Pleural effusion, fetal 0.56% (1/178 anomalies), in case MDB324
• Ascites, fetal 0.56% (1/178 anomalies), in case MDB324
• Retroplacental hemorrhage 0.56% (1/178 anomalies), in case MDB324
• Neuronal migration anomaly 0.56% (1/178 anomalies), in case MDB336
• Polymicrogyria, diffuse 0.56% (1/178 anomalies), in case MDB336
• Absence of the pyramid tracts, bilateral 0.56% (1/178 anomalies), in case MDB336
• Partial agenesis of the corpus callosum (PACC) 0.56% (1/178 anomalies), in case MDB336
• Brachycephaly 0.56% (1/178 anomalies), in case MDB336
• Rocker-bottom feet 0.56% (1/178 anomalies), in case MDB336
• Splenomegaly, congenital 0.56% (1/178 anomalies), in case MDB336
• Dysplastic kidney with tubular cysts 0.56% (1/178 anomalies), in case MDB346
• Bladder hypoplasia 0.56% (1/178 anomalies), in case MDB346
• Tetralogy of Fallot 0.56% (1/178 anomalies), in case MDB346
• Pulmonary valve atresia 0.56% (1/178 anomalies), in case MDB346
• Pulmonary artery hypoplasia 0.56% (1/178 anomalies), in case MDB346
• Dextroposition of aorta 0.56% (1/178 anomalies), in case MDB346
• Right ventricular hypertrophy 0.56% (1/178 anomalies), in case MDB346
• Microtia 0.56% (1/178 anomalies), in case MDB346
• Malformed ear 0.56% (1/178 anomalies), in case MDB346
• Bulbous nose 0.56% (1/178 anomalies), in case MDB346
• Polydactyly,of the hand, postaxial 0.56% (1/178 anomalies), in case MDB346
• Syndactyly of the toes, complex, bilateral 0.56% (1/178 anomalies), in case MDB346
• Talipes equinovarus,unilateral 0.56% (1/178 anomalies), in case MDB346
• Meckel diverticulum 0.56% (1/178 anomalies), in case MDB346
• Nephromegaly, bilateral 0.56% (1/178 anomalies), in case MDB346
• Absence of Posterior Commissure 0.56% (1/178 anomalies), in case MDB351
• Absence of Anterior Commissure 0.56% (1/178 anomalies), in case MDB351
• Hydranencephaly 0.56% (1/178 anomalies), in case MDB351
• Infarcted placenta 0.56% (1/178 anomalies), in case MDB351
• Cortical dysgenesis (CD), diffuse 0.56% (1/178 anomalies), in case MDB351
• Turricephaly 0.56% (1/178 anomalies), in case MDB351
• Ambiguous genitalia 0.56% (1/178 anomalies), in case MDB372
• Micropenis 0.56% (1/178 anomalies), in case MDB372
• Diaphragmatic hernia,unilateral 0.56% (1/178 anomalies), in case MDB372
• Dextrocardia, isolated 0.56% (1/178 anomalies), in case MDB372
• Pulmonary artery dilatation, fetal 0.56% (1/178 anomalies), in case MDB372
• Large anterior fontanelle 0.56% (1/178 anomalies), in case MDB372
• Penile Scrotal Fusion 0.56% (1/178 anomalies), in case MDB372
• Bicornuate uterus 0.56% (1/178 anomalies), in case MDB372
• Hypoplastic scrotum 0.56% (1/178 anomalies), in case MDB372
• Ventricular septal defect, membranous 0.56% (1/178 anomalies), in case MDB388
• Single umblical artery (SUA)-Isolated 0.56% (1/178 anomalies), in case MDB388
• Retrognathia 0.56% (1/178 anomalies), in case MDB394
• Ureter hypoplasia 0.56% (1/178 anomalies), in case MDB394
• Stenosis of the mid ureter, congenital, left side 0.56% (1/178 anomalies), in case MDB394
• Hand edema 0.56% (1/178 anomalies), in case MDB394
• Foot edema 0.56% (1/178 anomalies), in case MDB394
• Hydrocephalus 0.56% (1/178 anomalies), in case MDB394
• Lumbosacral agenesis 0.56% (1/178 anomalies), in case MDB439
• Arnold-Chiari Type II malformation (CM II) 0.56% (1/178 anomalies), in case MDB439
• Tonsillar herniation of the cerebellum 0.56% (1/178 anomalies), in case MDB439
• Stenosis of aqueduct of Sylvius 0.56% (1/178 anomalies), in case MDB439
• Scaphoid abdomen 0.56% (1/178 anomalies), in case MDB439
• Hypoplasia of ascending aorta 0.56% (1/178 anomalies), in case MDB439
• Rachischisis 0.56% (1/178 anomalies), in case MDB439
• Myelomeningocele, lumbosacral 0.56% (1/178 anomalies), in case MDB439
• Hydromyelia 0.56% (1/178 anomalies), in case MDB439
• Hydrocephalus, Non-communicating 0.56% (1/178 anomalies), in case MDB439
• Rectovesical fistula 0.56% (1/178 anomalies), in case MDB462
• Overlapping fingers 0.56% (1/178 anomalies), in case MDB489
• Toe hypoplasia, first, bilateral 0.56% (1/178 anomalies), in case MDB489
• Ureterovesical junction stenosis 0.56% (1/178 anomalies), in case MDB489
• Penis edema 0.56% (1/178 anomalies), in case MDB500
• Intra-abdominal testicule 0.56% (1/178 anomalies), in case MDB500
• Intestinal dilatation, congenital 0.56% (1/178 anomalies), in case MDB519
• Microcolon 0.56% (1/178 anomalies), in case MDB519
• Megabladder-microcolon-intestinal hypoperistalsis syndrome 0.56% (1/178 anomalies), in case MDB519
• Epicanthus 0.56% (1/178 anomalies), in case MDB23
• Cystic hygroma 0.56% (1/178 anomalies), in case MDB76