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• () in cases MDB, MDB, MDB, MDB

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

• Facial dysmorphism 6.25% (10/160 anomalies), in cases MDB3, MDB24, MDB136, MDB319, MDB321, MDB331, MDB397, MDB410, MDB260, MDB270
• Low-set ears 6.25% (10/160 anomalies), in cases MDB136, MDB242, MDB268, MDB319, MDB321, MDB331, MDB387, MDB410, MDB260, MDB270
• Short neck 5.63% (9/160 anomalies), in cases MDB38, MDB268, MDB319, MDB331, MDB341, MDB387, MDB164, MDB260, MDB270
• Macroglossia 4.38% (7/160 anomalies), in cases MDB3, MDB24, MDB41, MDB38, MDB319, MDB341, MDB270
• Intrauterine growth retardation, symmetric 4.38% (7/160 anomalies), in cases MDB136, MDB190, MDB305, MDB321, MDB387, MDB164, MDB270
• Placenta hypoplasia 4.38% (7/160 anomalies), in cases MDB136, MDB242, MDB268, MDB272, MDB305, MDB321, MDB387
• Low nasal bridge 4.38% (7/160 anomalies), in cases MDB268, MDB305, MDB331, MDB387, MDB397, MDB410, MDB260
• Hypertelorism 3.75% (6/160 anomalies), in cases MDB128, MDB136, MDB197, MDB321, MDB331, MDB270
• Clindodactyly of 5th finger, bilateral 2.5% (4/160 anomalies), in cases MDB128, MDB319, MDB331, MDB387
• Epicanthus 1.88% (3/160 anomalies), in cases MDB24, MDB197, MDB341
• Mongoloid slope of the palpebral fissures 1.88% (3/160 anomalies), in cases MDB24, MDB197, MDB410
• Clindodactyly of 5th finger, unilateral 1.88% (3/160 anomalies), in cases MDB41, MDB136, MDB305
• Neck edema 1.88% (3/160 anomalies), in cases MDB92, MDB38, MDB321
• Talipes equinovarus, bilateral 1.88% (3/160 anomalies), in cases MDB117, MDB331, MDB341
• Retrognathia 1.88% (3/160 anomalies), in cases MDB136, MDB397, MDB270
• Micrognathia 1.88% (3/160 anomalies), in cases MDB230, MDB242, MDB305
• Atrioventricular - channel 1.88% (3/160 anomalies), in cases MDB345, MDB410, MDB260
• Cystic hygroma 1.25% (2/160 anomalies), in cases MDB16, MDB260
• Synophrys 1.25% (2/160 anomalies), in cases MDB24, MDB41
• Renal pelvis dilatation, unilateral 1.25% (2/160 anomalies), in cases MDB92, MDB321
• Coarctation of aorta, 1.25% (2/160 anomalies), in cases MDB136, MDB268
• Pulmonary artery dilatation, fetal 1.25% (2/160 anomalies), in cases MDB136, MDB525
• Right ventricle dilatation 1.25% (2/160 anomalies), in cases MDB136, MDB525
• Pulmonary hypoplasia 1.25% (2/160 anomalies), in cases MDB230, MDB268
• Toe hypoplasia, first, bilateral 1.25% (2/160 anomalies), in cases MDB242, MDB243
• Macrosomia 1.25% (2/160 anomalies), in cases MDB243, MDB525
• Brachycephaly 1.25% (2/160 anomalies), in cases MDB268, MDB331
• Microstomia 1.25% (2/160 anomalies), in cases MDB305, MDB341
• Ventricular septal defect, membranous 1.25% (2/160 anomalies), in cases MDB331, MDB387
• Microretrognathia 1.25% (2/160 anomalies), in cases MDB331, MDB410
• Long philtrum 1.25% (2/160 anomalies), in cases MDB397, MDB270
• Small round skull 0.63% (1/160 anomalies), in case MDB3
• Thumb duplication 0.63% (1/160 anomalies), in case MDB16
• Sloping forehead 0.63% (1/160 anomalies), in case MDB24
• Aortic valve stenosis, congenital 0.63% (1/160 anomalies), in case MDB136
• Defective developement of left ventricle 0.63% (1/160 anomalies), in case MDB136
• Right atrium Enlargement 0.63% (1/160 anomalies), in case MDB136
• Polydactyly of both fingers & toes, postaxial 0.63% (1/160 anomalies), in case MDB136
• Intestinal malrotation 0.63% (1/160 anomalies), in case MDB136
• Meckel diverticulum 0.63% (1/160 anomalies), in case MDB136
• Pleural effusion, fetal 0.63% (1/160 anomalies), in case MDB197
• cutaneous edema, fetal 0.63% (1/160 anomalies), in case MDB197
• Microcephaly 0.63% (1/160 anomalies), in case MDB38
• Cerebral ventriculomegaly 0.63% (1/160 anomalies), in case MDB38
• Communicating hydrocephalus 0.63% (1/160 anomalies), in case MDB38
• Arthrogryposis 0.63% (1/160 anomalies), in case MDB230
• Prominent and pointed nose 0.63% (1/160 anomalies), in case MDB242
• Wide space between 2nd and third fingers 0.63% (1/160 anomalies), in case MDB243
• Talipes equinovarus,unilateral 0.63% (1/160 anomalies), in case MDB243
• Duodenal atresia and stenosis, congenital 0.63% (1/160 anomalies), in case MDB243
• Aberrant right subclavian artery 0.63% (1/160 anomalies), in case MDB268
• Brachydactyly 0.63% (1/160 anomalies), in case MDB305
• Wide space between 1st and 2nd toes, bilateral 0.63% (1/160 anomalies), in case MDB305
• short nose 0.63% (1/160 anomalies), in case MDB319
• Levocardia 0.63% (1/160 anomalies), in case MDB319
• Broad nasal bridge 0.63% (1/160 anomalies), in case MDB321
• Pterygium colli 0.63% (1/160 anomalies), in case MDB321
• Hexadactyly, postaxial 0.63% (1/160 anomalies), in case MDB321
• Subcapsular renal cyst, 0.63% (1/160 anomalies), in case MDB341
• Dilatation of ureter , bilateral, congenital 0.63% (1/160 anomalies), in case MDB341
• Asplenia 0.63% (1/160 anomalies), in case MDB345
• Double Outlet Right Ventricle, Without Transposition and VSD 0.63% (1/160 anomalies), in case MDB345
• Common atrium 0.63% (1/160 anomalies), in case MDB345
• Trilobate lung, bilateral 0.63% (1/160 anomalies), in case MDB345
• Arnold-Chiari Type II malformation (CM II) 0.63% (1/160 anomalies), in case MDB397
• Myelomeningocele, lumbosacral 0.63% (1/160 anomalies), in case MDB397
• Microtia 0.63% (1/160 anomalies), in case MDB410
• Cardiomegaly, fetal 0.63% (1/160 anomalies), in case MDB525
• Aortic isthmus stenosis 0.63% (1/160 anomalies), in case MDB525
• Nonimmune hydrops fetalis (NIHF) 0.63% (1/160 anomalies), in case MDB164
• Foot edema 0.63% (1/160 anomalies), in case MDB164
• Micro Multicystic kidneys, medullary type 0.63% (1/160 anomalies), in case MDB260