Malformations.org

Synonyms:

• Congenital megaloureter

• () in case MDB

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

• Renal pelvis dilatation, bilateral 4.42% (8/181 anomalies), in cases MDB23, MDB320, MDB388, MDB439, MDB462, MDB500, MDB519, MDB324
• Flattened nose 3.31% (6/181 anomalies), in cases MDB255, MDB320, MDB429, MDB500, MDB329, MDB324
• Megacystis 3.31% (6/181 anomalies), in cases MDB320, MDB429, MDB500, MDB519, MDB329, MDB324
• Facial dysmorphism 2.76% (5/181 anomalies), in cases MDB5, MDB125, MDB320, MDB439, MDB329
• Hydronephrosis, congenital, bilateral 2.76% (5/181 anomalies), in cases MDB23, MDB320, MDB432, MDB500, MDB329
• Pulmonary hypoplasia 2.76% (5/181 anomalies), in cases MDB23, MDB125, MDB388, MDB329, MDB324
• Epicanthus 2.21% (4/181 anomalies), in cases MDB5, MDB23, MDB125, MDB341
• Potter deformity sequence 2.21% (4/181 anomalies), in cases MDB255, MDB429, MDB500, MDB324
• Short neck 2.21% (4/181 anomalies), in cases MDB320, MDB432, MDB329, MDB341
• Macroglossia 1.66% (3/181 anomalies), in cases MDB5, MDB432, MDB341
• Transverse palmar crease, bilateral 1.66% (3/181 anomalies), in cases MDB5, MDB125, MDB432
• Talipes equinovarus, bilateral 1.66% (3/181 anomalies), in cases MDB5, MDB324, MDB341
• Bladder wall thickness 1.66% (3/181 anomalies), in cases MDB5, MDB320, MDB462
• Multicystic renal dysplasia,bilateral 1.66% (3/181 anomalies), in cases MDB23, MDB255, MDB320
• Hypertelorism 1.66% (3/181 anomalies), in cases MDB125, MDB320, MDB439
• Potter's facies 1.66% (3/181 anomalies), in cases MDB255, MDB500, MDB324
• Placenta hypoplasia 1.66% (3/181 anomalies), in cases MDB255, MDB320, MDB329
• Megarectum 1.66% (3/181 anomalies), in cases MDB255, MDB439, MDB462
• Imperforate Anus 1.66% (3/181 anomalies), in cases MDB255, MDB439, MDB462
• Lobulated, fused and horseshoe kidney 1.66% (3/181 anomalies), in cases MDB320, MDB439, MDB462
• Long philtrum 1.66% (3/181 anomalies), in cases MDB320, MDB329, MDB324
• Micrognathia 1.66% (3/181 anomalies), in cases MDB320, MDB500, MDB324
• Ventricular septal defect, membranous 1.1% (2/181 anomalies), in cases MDB5, MDB388
• Intestinal malrotation 1.1% (2/181 anomalies), in cases MDB5, MDB125
• Cystic hygroma 1.1% (2/181 anomalies), in cases MDB5, MDB329
• Clindodactyly of 5th finger, bilateral 1.1% (2/181 anomalies), in cases MDB23, MDB324
• Bladder dilatation, fetal 1.1% (2/181 anomalies), in cases MDB255, MDB462
• Posterior urethral valves, congenital 1.1% (2/181 anomalies), in cases MDB320, MDB500
• Broad nasal bridge 1.1% (2/181 anomalies), in cases MDB320, MDB439
• Posteriorly inclined and low-positioned ears 1.1% (2/181 anomalies), in cases MDB320, MDB324
• Microstomia 1.1% (2/181 anomalies), in cases MDB320, MDB341
• Intrauterine growth retardation, symmetric 1.1% (2/181 anomalies), in cases MDB388, MDB329
• Hepatomegaly, fetal 1.1% (2/181 anomalies), in cases MDB429, MDB519
• Low nasal bridge 1.1% (2/181 anomalies), in cases MDB432, MDB324
• Hydromyelia 1.1% (2/181 anomalies), in cases MDB439, MDB329
• Polymicrogyria, focal 1.1% (2/181 anomalies), in cases MDB329, MDB329
• Flat face 0.55% (1/181 anomalies), in case MDB5
• Flattened occiput 0.55% (1/181 anomalies), in case MDB5
• Atrial Hypertrophy 0.55% (1/181 anomalies), in case MDB5
• Overlapping toes 0.55% (1/181 anomalies), in case MDB5
• Preauricular hamartoma 0.55% (1/181 anomalies), in case MDB5
• Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.55% (1/181 anomalies), in case MDB5
• Fusion of the adrenal glands 0.55% (1/181 anomalies), in case MDB5
• Microsplenia 0.55% (1/181 anomalies), in case MDB5
• Lung agenesis, unilateral 0.55% (1/181 anomalies), in case MDB5
• Unilobate lung, unilateral 0.55% (1/181 anomalies), in case MDB5
• Amnion nodosum 0.55% (1/181 anomalies), in case MDB5
• Polysplenia 0.55% (1/181 anomalies), in case MDB5
• Atrioventricular - channel 0.55% (1/181 anomalies), in case MDB125
• Coarctation of aorta, 0.55% (1/181 anomalies), in case MDB125
• Hypoplasia of the aortic isthmus 0.55% (1/181 anomalies), in case MDB125
• Defective developement of left ventricle 0.55% (1/181 anomalies), in case MDB125
• Nonimmune hydrops fetalis (NIHF) 0.55% (1/181 anomalies), in case MDB125
• Macrocephaly 0.55% (1/181 anomalies), in case MDB125
• Retrognathia 0.55% (1/181 anomalies), in case MDB255
• Macrosomia 0.55% (1/181 anomalies), in case MDB255
• Cloacal dysgenesis sequence (CDS) 0.55% (1/181 anomalies), in case MDB255
• Badly-hemmed ears 0.55% (1/181 anomalies), in case MDB320
• Thin upper lip 0.55% (1/181 anomalies), in case MDB320
• Gothic palate 0.55% (1/181 anomalies), in case MDB320
• Cleft palate, median posterior 0.55% (1/181 anomalies), in case MDB320
• Hypospadias, Glandular 0.55% (1/181 anomalies), in case MDB320
• Single umblical artery (SUA)-Isolated 0.55% (1/181 anomalies), in case MDB388
• Distended abdomen, fetal 0.55% (1/181 anomalies), in case MDB429
• Palpebral edema, bilateral 0.55% (1/181 anomalies), in case MDB429
• Cubital deviation of the hand, bilateral 0.55% (1/181 anomalies), in case MDB429
• Brachydactyly of the toes 0.55% (1/181 anomalies), in case MDB432
• Lumbosacral agenesis 0.55% (1/181 anomalies), in case MDB439
• Arnold-Chiari Type II malformation (CM II) 0.55% (1/181 anomalies), in case MDB439
• Tonsillar herniation of the cerebellum 0.55% (1/181 anomalies), in case MDB439
• Stenosis of aqueduct of Sylvius 0.55% (1/181 anomalies), in case MDB439
• Scaphoid abdomen 0.55% (1/181 anomalies), in case MDB439
• Hypoplasia of ascending aorta 0.55% (1/181 anomalies), in case MDB439
• Rachischisis 0.55% (1/181 anomalies), in case MDB439
• Myelomeningocele, lumbosacral 0.55% (1/181 anomalies), in case MDB439
• Hydrocephalus, Non-communicating 0.55% (1/181 anomalies), in case MDB439
• Rectovesical fistula 0.55% (1/181 anomalies), in case MDB462
• Hypospadias, penile 0.55% (1/181 anomalies), in case MDB462
• Penis edema 0.55% (1/181 anomalies), in case MDB500
• Intra-abdominal testicule 0.55% (1/181 anomalies), in case MDB500
• Intestinal dilatation, congenital 0.55% (1/181 anomalies), in case MDB519
• Microcolon 0.55% (1/181 anomalies), in case MDB519
• Megabladder-microcolon-intestinal hypoperistalsis syndrome 0.55% (1/181 anomalies), in case MDB519
• Microcephaly 0.55% (1/181 anomalies), in case MDB329
• Holoprosencephaly, lobar 0.55% (1/181 anomalies), in case MDB329
• Thalamic nuclei centrum medianum fusion 0.55% (1/181 anomalies), in case MDB329
• Corpus callosum agenesis 0.55% (1/181 anomalies), in case MDB329
• Hypogenesis of the Cerebellar Vermis 0.55% (1/181 anomalies), in case MDB329
• Cerebellar hypoplasia 0.55% (1/181 anomalies), in case MDB329
• Low-set ears 0.55% (1/181 anomalies), in case MDB329
• Prominent upper lip 0.55% (1/181 anomalies), in case MDB329
• Arthrogryposis 0.55% (1/181 anomalies), in case MDB329
• Micromelia, lower limb, unilateral 0.55% (1/181 anomalies), in case MDB329
• Ventricular septal defect, muscular 0.55% (1/181 anomalies), in case MDB329
• Hypoplasia and dysplasia of the kidney, bilateral 0.55% (1/181 anomalies), in case MDB324
• Sloping forehead 0.55% (1/181 anomalies), in case MDB324
• Neck edema 0.55% (1/181 anomalies), in case MDB324
• Pericardial effusion 0.55% (1/181 anomalies), in case MDB324
• Pleural effusion, fetal 0.55% (1/181 anomalies), in case MDB324
• Ascites, fetal 0.55% (1/181 anomalies), in case MDB324
• Retroplacental hemorrhage 0.55% (1/181 anomalies), in case MDB324
• Single transverse palmar crease, unilateral 0.55% (1/181 anomalies), in case MDB341
• Subcapsular renal cyst, 0.55% (1/181 anomalies), in case MDB341