Malformations.org

• () in case MDB

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

• Low-set ears 5.88% (4/68 anomalies), in cases MDB29, MDB53, MDB473, MDB491
• Placenta hypoplasia 5.88% (4/68 anomalies), in cases MDB29, MDB473, MDB491, MDB492
• Facial dysmorphism 4.41% (3/68 anomalies), in cases MDB29, MDB53, MDB473
• Intrauterine growth retardation, symmetric 4.41% (3/68 anomalies), in cases MDB53, MDB158, MDB473
• Pulmonary hypoplasia 2.94% (2/68 anomalies), in cases MDB29, MDB529
• Talipes equinovarus, bilateral 2.94% (2/68 anomalies), in cases MDB29, MDB158
• Single umblical artery (SUA)-Isolated 2.94% (2/68 anomalies), in cases MDB53, MDB492
• hypoplasia of the rib 2.94% (2/68 anomalies), in cases MDB53, MDB473
• Coarctation of aorta, 2.94% (2/68 anomalies), in cases MDB53, MDB529
• Hypertelorism 2.94% (2/68 anomalies), in cases MDB473, MDB491
• Tetralogy of Fallot 2.94% (2/68 anomalies), in cases MDB491, MDB492
• Cleft palate, bilateral, complete 1.47% (1/68 anomalies), in case MDB25
• Multicystic renal dysplasia,bilateral 1.47% (1/68 anomalies), in case MDB29
• Epicanthus 1.47% (1/68 anomalies), in case MDB29
• Long philtrum 1.47% (1/68 anomalies), in case MDB29
• Neck edema 1.47% (1/68 anomalies), in case MDB29
• Foot edema 1.47% (1/68 anomalies), in case MDB29
• Axillary pterygia,unilateral 1.47% (1/68 anomalies), in case MDB29
• Tridactyly, unilateral 1.47% (1/68 anomalies), in case MDB29
• vertebral bones and gracile ribs with multiple abnormalities 1.47% (1/68 anomalies), in case MDB29
• Ventricular septal defect, muscular 1.47% (1/68 anomalies), in case MDB53
• Renal pelvis dilatation, unilateral 1.47% (1/68 anomalies), in case MDB53
• Lobulated, fused and horseshoe kidney 1.47% (1/68 anomalies), in case MDB53
• Radial ray agenesis, unilateral 1.47% (1/68 anomalies), in case MDB53
• Syndactyly, simple (webbed), fingers 1.47% (1/68 anomalies), in case MDB53
• Clindodactyly of 5th finger, unilateral 1.47% (1/68 anomalies), in case MDB53
• Large anterior fontanelle 1.47% (1/68 anomalies), in case MDB53
• Triangular face 1.47% (1/68 anomalies), in case MDB53
• Overlapping fingers 1.47% (1/68 anomalies), in case MDB158
• Microcephaly 1.47% (1/68 anomalies), in case MDB473
• Semilobar holoprosencephaly 1.47% (1/68 anomalies), in case MDB473
• Corpus callosum agenesis 1.47% (1/68 anomalies), in case MDB473
• Deep gray nuclear malformations(the caudate nuclei, thalami,..) 1.47% (1/68 anomalies), in case MDB473
• Incomplete cleavage of cerebral hemispheres 1.47% (1/68 anomalies), in case MDB473
• Single cerebral ventricule 1.47% (1/68 anomalies), in case MDB473
• Short philtrum 1.47% (1/68 anomalies), in case MDB473
• Micrognathia 1.47% (1/68 anomalies), in case MDB473
• Myelomeningocele,thoracolumbar 1.47% (1/68 anomalies), in case MDB473
• Polydactyly,of the hand, postaxial 1.47% (1/68 anomalies), in case MDB473
• Polydactyly of the hand, preaxial 1.47% (1/68 anomalies), in case MDB473
• Pulmonary valve dysplasia 1.47% (1/68 anomalies), in case MDB473
• Tricuspid valve dysplasia 1.47% (1/68 anomalies), in case MDB473
• Interauricular communication 1.47% (1/68 anomalies), in case MDB473
• Hypoplasia of diaphragm 1.47% (1/68 anomalies), in case MDB491
• Short umbilical cord 1.47% (1/68 anomalies), in case MDB491
• Imperforate Anus 1.47% (1/68 anomalies), in case MDB492
• Renal ectopia,crossed 1.47% (1/68 anomalies), in case MDB492
• Microretrognathia 1.47% (1/68 anomalies), in case MDB529
• Flattened nose 1.47% (1/68 anomalies), in case MDB529
• Pulmonary artery dilatation, fetal 1.47% (1/68 anomalies), in case MDB529
• Right ventricular hypertrophy 1.47% (1/68 anomalies), in case MDB529