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• () in case MDB

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

• Pulmonary hypoplasia 3.65% (7/192 anomalies), in cases MDB23, MDB29, MDB67, MDB181, MDB409, MDB496, MDB150
• Placenta hypoplasia 3.13% (6/192 anomalies), in cases MDB29, MDB215, MDB255, MDB278, MDB320, MDB496
• Hypertelorism 2.6% (5/192 anomalies), in cases MDB20, MDB67, MDB181, MDB215, MDB320
• Talipes equinovarus, bilateral 2.6% (5/192 anomalies), in cases MDB29, MDB181, MDB215, MDB418, MDB150
• Facial dysmorphism 2.6% (5/192 anomalies), in cases MDB29, MDB215, MDB278, MDB320, MDB418
• Single umblical artery (SUA)-Isolated 2.6% (5/192 anomalies), in cases MDB215, MDB278, MDB418, MDB496, MDB262
• Low-set ears 2.08% (4/192 anomalies), in cases MDB29, MDB181, MDB215, MDB150
• Potter deformity sequence 2.08% (4/192 anomalies), in cases MDB181, MDB255, MDB409, MDB150
• Imperforate Anus 2.08% (4/192 anomalies), in cases MDB255, MDB409, MDB150, MDB262
• Dilatation of ureter , bilateral, congenital 1.56% (3/192 anomalies), in cases MDB23, MDB255, MDB320
• Hydronephrosis, congenital, bilateral 1.56% (3/192 anomalies), in cases MDB23, MDB71, MDB320
• Long philtrum 1.56% (3/192 anomalies), in cases MDB29, MDB320, MDB150
• Broad nasal bridge 1.56% (3/192 anomalies), in cases MDB181, MDB215, MDB320
• Bladder hypoplasia 1.56% (3/192 anomalies), in cases MDB181, MDB278, MDB418
• Polysplenia 1.56% (3/192 anomalies), in cases MDB181, MDB150, MDB262
• Short neck 1.56% (3/192 anomalies), in cases MDB215, MDB320, MDB496
• Intrauterine growth retardation, symmetric 1.56% (3/192 anomalies), in cases MDB215, MDB278, MDB418
• Potter's facies 1.56% (3/192 anomalies), in cases MDB255, MDB409, MDB150
• Posteriorly inclined and low-positioned ears 1.56% (3/192 anomalies), in cases MDB320, MDB418, MDB496
• Clindodactyly of 5th finger, bilateral 1.04% (2/192 anomalies), in cases MDB23, MDB215
• Epicanthus 1.04% (2/192 anomalies), in cases MDB23, MDB29
• Renal pelvis dilatation, bilateral 1.04% (2/192 anomalies), in cases MDB23, MDB320
• Neck edema 1.04% (2/192 anomalies), in cases MDB29, MDB496
• vertebral bones and gracile ribs with multiple abnormalities 1.04% (2/192 anomalies), in cases MDB29, MDB150
• Retroplacental hemorrhage 1.04% (2/192 anomalies), in cases MDB71, MDB150
• Nephromegaly, bilateral 1.04% (2/192 anomalies), in cases MDB181, MDB278
• Ureter hypoplasia 1.04% (2/192 anomalies), in cases MDB181, MDB418
• Cleft palate, median posterior 1.04% (2/192 anomalies), in cases MDB215, MDB320
• Retrognathia 1.04% (2/192 anomalies), in cases MDB255, MDB262
• Cloacal dysgenesis sequence (CDS) 1.04% (2/192 anomalies), in cases MDB255, MDB262
• Flattened nose 1.04% (2/192 anomalies), in cases MDB255, MDB320
• Camptodactyly, unilateral 1.04% (2/192 anomalies), in cases MDB278, MDB496
• Long umbilical cord 1.04% (2/192 anomalies), in cases MDB278, MDB150
• Lobulated, fused and horseshoe kidney 1.04% (2/192 anomalies), in cases MDB320, MDB262
• Gothic palate 1.04% (2/192 anomalies), in cases MDB320, MDB496
• Micrognathia 1.04% (2/192 anomalies), in cases MDB320, MDB262
• Renal agenesis, unilateral 1.04% (2/192 anomalies), in cases MDB409, MDB150
• Right aortic arch 1.04% (2/192 anomalies), in cases MDB409, MDB418
• Polydactyly of both fingers & toes, postaxial 0.52% (1/192 anomalies), in case MDB20
• Sloping forehead 0.52% (1/192 anomalies), in case MDB20
• Giant omphalocele 0.52% (1/192 anomalies), in case MDB29
• Foot edema 0.52% (1/192 anomalies), in case MDB29
• Axillary pterygia,unilateral 0.52% (1/192 anomalies), in case MDB29
• Tridactyly, unilateral 0.52% (1/192 anomalies), in case MDB29
• Oligohydramnios 0.52% (1/192 anomalies), in case MDB67
• Cerebral ventriculomegaly 0.52% (1/192 anomalies), in case MDB71
• Encephalocele, occipital 0.52% (1/192 anomalies), in case MDB181
• Olfactory bulbs, absence of 0.52% (1/192 anomalies), in case MDB181
• Periventricular heterotopia (PH) 0.52% (1/192 anomalies), in case MDB181
• Polymicrogyria, focal 0.52% (1/192 anomalies), in case MDB181
• Cerebellar hypoplasia 0.52% (1/192 anomalies), in case MDB181
• Low nasal bridge 0.52% (1/192 anomalies), in case MDB181
• Microretrognathia 0.52% (1/192 anomalies), in case MDB181
• Hexadactyly, postaxial 0.52% (1/192 anomalies), in case MDB181
• Renal-hepatic-pancreatic dysplasia 0.52% (1/192 anomalies), in case MDB181
• Deep gray nuclear malformations(the caudate nuclei, thalami,..) 0.52% (1/192 anomalies), in case MDB181
• putamen nuclei absence 0.52% (1/192 anomalies), in case MDB181
• Glial heterotopia, multi-focal 0.52% (1/192 anomalies), in case MDB181
• Corticospinal tract absence 0.52% (1/192 anomalies), in case MDB181
• Micromelia 0.52% (1/192 anomalies), in case MDB215
• Microphthalmia 0.52% (1/192 anomalies), in case MDB215
• Right bilobate lung 0.52% (1/192 anomalies), in case MDB215
• Unilobate lung, unilateral 0.52% (1/192 anomalies), in case MDB215
• Macrosomia 0.52% (1/192 anomalies), in case MDB255
• Bladder dilatation, fetal 0.52% (1/192 anomalies), in case MDB255
• Megarectum 0.52% (1/192 anomalies), in case MDB255
• Hypogenesis of the Cerebellar Vermis 0.52% (1/192 anomalies), in case MDB278
• Spina bifida occulta, lombosacral 0.52% (1/192 anomalies), in case MDB278
• Limbs hypoplasia 0.52% (1/192 anomalies), in case MDB278
• Syndactyly of the toes, unilateral 0.52% (1/192 anomalies), in case MDB278
• Megacystis 0.52% (1/192 anomalies), in case MDB320
• Posterior urethral valves, congenital 0.52% (1/192 anomalies), in case MDB320
• Bladder wall thickness 0.52% (1/192 anomalies), in case MDB320
• Badly-hemmed ears 0.52% (1/192 anomalies), in case MDB320
• Microstomia 0.52% (1/192 anomalies), in case MDB320
• Thin upper lip 0.52% (1/192 anomalies), in case MDB320
• Hypospadias, Glandular 0.52% (1/192 anomalies), in case MDB320
• Lumbosacral agenesis 0.52% (1/192 anomalies), in case MDB409
• Sirenomelia 0.52% (1/192 anomalies), in case MDB409
• Bladder agenesis 0.52% (1/192 anomalies), in case MDB409
• Agenesia of internal genital organs 0.52% (1/192 anomalies), in case MDB409
• Dextrocardia with Situs Inversus 0.52% (1/192 anomalies), in case MDB409
• Stenosis of aqueduct of Sylvius 0.52% (1/192 anomalies), in case MDB409
• Hydrocephalus, Non-communicating 0.52% (1/192 anomalies), in case MDB409
• Absence of the Septum Pellucidum 0.52% (1/192 anomalies), in case MDB409
• Arthrogryposis 0.52% (1/192 anomalies), in case MDB409
• Dextrocardia, isolated 0.52% (1/192 anomalies), in case MDB418
• Persistent left superior vena cava 0.52% (1/192 anomalies), in case MDB418
• Unicorn Uterus 0.52% (1/192 anomalies), in case MDB418
• Fallopian tube, absence of 0.52% (1/192 anomalies), in case MDB418
• Pulmonary artery hypoplasia 0.52% (1/192 anomalies), in case MDB418
• Ventricular septal defect, muscular 0.52% (1/192 anomalies), in case MDB418
• Cleft palate with cleft lip,bilateral, complete 0.52% (1/192 anomalies), in case MDB418
• Anencephaly 0.52% (1/192 anomalies), in case MDB496
• Anencephaly facies 0.52% (1/192 anomalies), in case MDB496
• Exophthalmos, bilateral 0.52% (1/192 anomalies), in case MDB496
• Macroglossia 0.52% (1/192 anomalies), in case MDB496
• Ambiguous genitalia 0.52% (1/192 anomalies), in case MDB150
• Flat face 0.52% (1/192 anomalies), in case MDB150
• Microcephaly 0.52% (1/192 anomalies), in case MDB150
• Axillary pterygia, bilateral 0.52% (1/192 anomalies), in case MDB150
• Hand edema 0.52% (1/192 anomalies), in case MDB150
• Toe hypoplasia, first, bilateral 0.52% (1/192 anomalies), in case MDB150
• Wide space between 1st and 2nd toes, bilateral 0.52% (1/192 anomalies), in case MDB150
• Persistent cloaca 0.52% (1/192 anomalies), in case MDB150
• Malpositioned thumb, bilateral 0.52% (1/192 anomalies), in case MDB150
• Ureter agenesis, unilateral 0.52% (1/192 anomalies), in case MDB150
• Duodenal atresia and stenosis, congenital 0.52% (1/192 anomalies), in case MDB262
• Rectovesical fistula 0.52% (1/192 anomalies), in case MDB262
• Crossed fused renal ectopia 0.52% (1/192 anomalies), in case MDB262
• Renal hypoplasia, unilateral 0.52% (1/192 anomalies), in case MDB262
• Hydronephrosis, congenital, unilateral 0.52% (1/192 anomalies), in case MDB262
• Hydroureter, unilateral 0.52% (1/192 anomalies), in case MDB262
• Hypospadias, penile 0.52% (1/192 anomalies), in case MDB262
• Coarctation of aorta, 0.52% (1/192 anomalies), in case MDB262
• Pulmonary lobation anomalies 0.52% (1/192 anomalies), in case MDB262
• Placental hypermaturity 0.52% (1/192 anomalies), in case MDB262