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

• Facial dysmorphism 3.62% (5/138 anomalies), in cases MDB37, MDB402, MDB261, MDB418, MDB459
• Pulmonary hypoplasia 3.62% (5/138 anomalies), in cases MDB37, MDB277, MDB417, MDB326, MDB261
• Placenta hypoplasia 3.62% (5/138 anomalies), in cases MDB37, MDB417, MDB326, MDB261, MDB301
• Low-set ears 2.9% (4/138 anomalies), in cases MDB402, MDB326, MDB261, MDB459
• Hypotelorisme 2.17% (3/138 anomalies), in cases MDB37, MDB326, MDB14
• Micropenis 2.17% (3/138 anomalies), in cases MDB37, MDB402, MDB326
• Polydactyly of both fingers & toes, postaxial 1.45% (2/138 anomalies), in cases MDB37, MDB459
• Nephromegaly, bilateral 1.45% (2/138 anomalies), in cases MDB37, MDB459
• Meckel diverticulum 1.45% (2/138 anomalies), in cases MDB37, MDB326
• Holoprosencephaly, alobar 1.45% (2/138 anomalies), in cases MDB37, MDB14
• Thalamic nuclei centrum medianum fusion 1.45% (2/138 anomalies), in cases MDB37, MDB14
• Corpus callosum agenesis 1.45% (2/138 anomalies), in cases MDB37, MDB14
• Omphalocele 1.45% (2/138 anomalies), in cases MDB277, MDB94
• Retroplacental hemorrhage 1.45% (2/138 anomalies), in cases MDB277, MDB326
• Fingers amputation 1.45% (2/138 anomalies), in cases MDB277, MDB94
• Intrauterine growth retardation, symmetric 1.45% (2/138 anomalies), in cases MDB277, MDB418
• Intestinal malrotation 1.45% (2/138 anomalies), in cases MDB402, MDB301
• Talipes equinovarus, bilateral 1.45% (2/138 anomalies), in cases MDB417, MDB418
• Microcephaly 1.45% (2/138 anomalies), in cases MDB326, MDB14
• Pulmonary artery hypoplasia 1.45% (2/138 anomalies), in cases MDB326, MDB418
• Hypertelorism 1.45% (2/138 anomalies), in cases MDB94, MDB459
• Myelomeningocele, lumbosacral 0.72% (1/138 anomalies), in case MDB37
• Flat face 0.72% (1/138 anomalies), in case MDB37
• Rachischisis 0.72% (1/138 anomalies), in case MDB37
• Splenomegaly, congenital 0.72% (1/138 anomalies), in case MDB37
• Microtia 0.72% (1/138 anomalies), in case MDB37
• Semilobar holoprosencephaly 0.72% (1/138 anomalies), in case MDB277
• Prominent infraorbital creases 0.72% (1/138 anomalies), in case MDB277
• Ectopia cordis 0.72% (1/138 anomalies), in case MDB277
• Exencephaly 0.72% (1/138 anomalies), in case MDB277
• Enophtalmus 0.72% (1/138 anomalies), in case MDB277
• Congenital Muscular Torticollis, Fetal 0.72% (1/138 anomalies), in case MDB277
• Placental amniotic bands 0.72% (1/138 anomalies), in case MDB277
• Diaphragmatic hernia, congenital 0.72% (1/138 anomalies), in case MDB277
• Retrognathia 0.72% (1/138 anomalies), in case MDB402
• Fraser syndrome 0.72% (1/138 anomalies), in case MDB402
• Toe hypoplasia, first, bilateral 0.72% (1/138 anomalies), in case MDB402
• Subglottic Stenosis (CSS) 0.72% (1/138 anomalies), in case MDB402
• Non-segmented lung 0.72% (1/138 anomalies), in case MDB402
• Ureter agenesis, bilateral 0.72% (1/138 anomalies), in case MDB402
• Renal agenesis, bilateral 0.72% (1/138 anomalies), in case MDB402
• Bladder agenesis 0.72% (1/138 anomalies), in case MDB402
• Left side appendix 0.72% (1/138 anomalies), in case MDB402
• Imperforate Anus 0.72% (1/138 anomalies), in case MDB402
• Coarctation of aorta, 0.72% (1/138 anomalies), in case MDB402
• Pyloric stenosis 0.72% (1/138 anomalies), in case MDB402
• Amnion nodosum 0.72% (1/138 anomalies), in case MDB402
• Syndactyly of the fingers, complex, bilateral 0.72% (1/138 anomalies), in case MDB402
• Arnold-Chiari Type II malformation (CM II) 0.72% (1/138 anomalies), in case MDB417
• Nasal hypoplasia 0.72% (1/138 anomalies), in case MDB417
• Lobulated, fused and horseshoe kidney 0.72% (1/138 anomalies), in case MDB417
• Flattened occiput 0.72% (1/138 anomalies), in case MDB417
• Short neck 0.72% (1/138 anomalies), in case MDB417
• Myelomeningocele,lumbosacral with hydrocephalus 0.72% (1/138 anomalies), in case MDB417
• Interauricular communication 0.72% (1/138 anomalies), in case MDB326
• Sloping forehead 0.72% (1/138 anomalies), in case MDB326
• Badly-hemmed ears 0.72% (1/138 anomalies), in case MDB326
• Broad nasal bridge 0.72% (1/138 anomalies), in case MDB326
• Microretrognathia 0.72% (1/138 anomalies), in case MDB326
• Hexadactyly, postaxial 0.72% (1/138 anomalies), in case MDB326
• Tetralogy of Fallot 0.72% (1/138 anomalies), in case MDB326
• Dextroposition of aorta 0.72% (1/138 anomalies), in case MDB326
• Ventricular septal defect, membranous 0.72% (1/138 anomalies), in case MDB326
• Right atrium Enlargement 0.72% (1/138 anomalies), in case MDB326
• Thymic hypoplasia 0.72% (1/138 anomalies), in case MDB326
• Polysplenia 0.72% (1/138 anomalies), in case MDB326
• Absence of one paire the rib 0.72% (1/138 anomalies), in case MDB326
• Absence of the pyramid tracts, bilateral 0.72% (1/138 anomalies), in case MDB14
• Hypogenesis of the Cerebellar Vermis 0.72% (1/138 anomalies), in case MDB14
• Obstetrician's hand 0.72% (1/138 anomalies), in case MDB14
• Polymicrogyria, focal 0.72% (1/138 anomalies), in case MDB14
• Syndactyly, simple (webbed), fingers 0.72% (1/138 anomalies), in case MDB94
• Cubital pterygium, bilateral 0.72% (1/138 anomalies), in case MDB94
• Anophthalmos, bilateral 0.72% (1/138 anomalies), in case MDB94
• Neck edema 0.72% (1/138 anomalies), in case MDB94
• Right bilobate lung 0.72% (1/138 anomalies), in case MDB94
• Transverse amputation of limb 0.72% (1/138 anomalies), in case MDB94
• Toes amputation 0.72% (1/138 anomalies), in case MDB94
• Syndactyly of the toes, complex, bilateral 0.72% (1/138 anomalies), in case MDB94
• overlapping skull bones 0.72% (1/138 anomalies), in case MDB94
• Thorax deformation,fetal 0.72% (1/138 anomalies), in case MDB94
• Open bite mouth, fetal 0.72% (1/138 anomalies), in case MDB94
• Acrocephaly 0.72% (1/138 anomalies), in case MDB261
• Arhinia 0.72% (1/138 anomalies), in case MDB261
• Microphthalmia 0.72% (1/138 anomalies), in case MDB261
• Decreased skull bone mineralization 0.72% (1/138 anomalies), in case MDB261
• Polydactyly,of the hand, postaxial 0.72% (1/138 anomalies), in case MDB301
• Hypoplasia of ascending aorta 0.72% (1/138 anomalies), in case MDB301
• Aberrant left subclavian artery 0.72% (1/138 anomalies), in case MDB301
• Bicornuate uterus 0.72% (1/138 anomalies), in case MDB301
• Bladder hypoplasia 0.72% (1/138 anomalies), in case MDB418
• Multicystic renal dysplasia,bilateral 0.72% (1/138 anomalies), in case MDB418
• Right aortic arch 0.72% (1/138 anomalies), in case MDB418
• Ureter hypoplasia 0.72% (1/138 anomalies), in case MDB418
• Dextrocardia, isolated 0.72% (1/138 anomalies), in case MDB418
• Persistent left superior vena cava 0.72% (1/138 anomalies), in case MDB418
• Unicorn Uterus 0.72% (1/138 anomalies), in case MDB418
• Fallopian tube, absence of 0.72% (1/138 anomalies), in case MDB418
• Posteriorly inclined and low-positioned ears 0.72% (1/138 anomalies), in case MDB418
• Single umblical artery (SUA)-Isolated 0.72% (1/138 anomalies), in case MDB418
• Ventricular septal defect, muscular 0.72% (1/138 anomalies), in case MDB418
• Hypospadias, penile 0.72% (1/138 anomalies), in case MDB459
• Adrenal hypoplasia, fetal 0.72% (1/138 anomalies), in case MDB459
• Micromulticystic kidneys 0.72% (1/138 anomalies), in case MDB459