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

• Corpus callosum agenesis 4.3% (8/186 anomalies), in cases MDB14, MDB37, MDB54, MDB291, MDB258, MDB329, MDB263, MDB469
• Microcephaly 3.76% (7/186 anomalies), in cases MDB14, MDB54, MDB291, MDB258, MDB329, MDB68, MDB263
• Facial dysmorphism 3.76% (7/186 anomalies), in cases MDB37, MDB54, MDB258, MDB329, MDB68, MDB263, MDB340
• Intrauterine growth retardation, symmetric 3.23% (6/186 anomalies), in cases MDB18, MDB161, MDB291, MDB329, MDB263, MDB340
• Placenta hypoplasia 3.23% (6/186 anomalies), in cases MDB37, MDB54, MDB291, MDB258, MDB329, MDB263
• Single cerebral ventricule 3.23% (6/186 anomalies), in cases MDB291, MDB258, MDB263, MDB340, MDB436, MDB469
• Holoprosencephaly, alobar 2.69% (5/186 anomalies), in cases MDB14, MDB18, MDB37, MDB68, MDB340
• Olfactory bulbs, absence of 2.69% (5/186 anomalies), in cases MDB54, MDB161, MDB291, MDB258, MDB340
• Microstomia 2.15% (4/186 anomalies), in cases MDB54, MDB291, MDB68, MDB340
• Olfactory nerve, absence of, bilateral 2.15% (4/186 anomalies), in cases MDB161, MDB291, MDB258, MDB340
• Hypotelorisme 1.61% (3/186 anomalies), in cases MDB14, MDB37, MDB68
• Polymicrogyria, focal 1.61% (3/186 anomalies), in cases MDB14, MDB329, MDB329
• Cyclopia 1.61% (3/186 anomalies), in cases MDB18, MDB291, MDB340
• Flat face 1.61% (3/186 anomalies), in cases MDB37, MDB68, MDB469
• Pulmonary hypoplasia 1.61% (3/186 anomalies), in cases MDB37, MDB291, MDB329
• Semilobar holoprosencephaly 1.61% (3/186 anomalies), in cases MDB54, MDB258, MDB469
• Trigonocephaly 1.61% (3/186 anomalies), in cases MDB161, MDB291, MDB340
• Holoprosencephaly, lobar 1.61% (3/186 anomalies), in cases MDB291, MDB329, MDB263
• Cerebellar hypoplasia 1.61% (3/186 anomalies), in cases MDB291, MDB329, MDB340
• Low-set ears 1.61% (3/186 anomalies), in cases MDB258, MDB329, MDB68
• Flattened nose 1.61% (3/186 anomalies), in cases MDB258, MDB329, MDB263
• Absence of the pyramid tracts, bilateral 1.08% (2/186 anomalies), in cases MDB14, MDB291
• Hypogenesis of the Cerebellar Vermis 1.08% (2/186 anomalies), in cases MDB14, MDB329
• Cleft palate with cleft lip,bilateral, complete 1.08% (2/186 anomalies), in cases MDB14, MDB37
• Micropenis 1.08% (2/186 anomalies), in cases MDB18, MDB37
• Polydactyly,of the hand, postaxial 1.08% (2/186 anomalies), in cases MDB18, MDB340
• Proboscis 1.08% (2/186 anomalies), in cases MDB18, MDB340
• Nephromegaly, bilateral 1.08% (2/186 anomalies), in cases MDB37, MDB68
• Optic nerve, absence of, bilateral 1.08% (2/186 anomalies), in cases MDB54, MDB340
• Anophthalmos, bilateral 1.08% (2/186 anomalies), in cases MDB54, MDB291
• Retrognathia 1.08% (2/186 anomalies), in cases MDB161, MDB436
• Toe hypoplasia, first, bilateral 1.08% (2/186 anomalies), in cases MDB161, MDB263
• Arhinia 1.08% (2/186 anomalies), in cases MDB291, MDB340
• Micrognathia 1.08% (2/186 anomalies), in cases MDB291, MDB263
• Hydronephrosis, congenital, bilateral 1.08% (2/186 anomalies), in cases MDB329, MDB340
• Long philtrum 1.08% (2/186 anomalies), in cases MDB329, MDB68
• Obstetrician's hand 0.54% (1/186 anomalies), in case MDB14
• Cortical dysgenesis (CD), diffuse 0.54% (1/186 anomalies), in case MDB18
• Myelomeningocele, lumbosacral 0.54% (1/186 anomalies), in case MDB37
• Polydactyly of both fingers & toes, postaxial 0.54% (1/186 anomalies), in case MDB37
• Rachischisis 0.54% (1/186 anomalies), in case MDB37
• Splenomegaly, congenital 0.54% (1/186 anomalies), in case MDB37
• Meckel diverticulum 0.54% (1/186 anomalies), in case MDB37
• Microtia 0.54% (1/186 anomalies), in case MDB37
• Microglossia 0.54% (1/186 anomalies), in case MDB54
• Holoprosencephaly 0.54% (1/186 anomalies), in case MDB161
• Hypertelorism 0.54% (1/186 anomalies), in case MDB161
• Overlapping fingers 0.54% (1/186 anomalies), in case MDB161
• Hypoplasia of optic nerve, bilateral 0.54% (1/186 anomalies), in case MDB291
• Arhinencephaly 0.54% (1/186 anomalies), in case MDB291
• Absence of neocortex 0.54% (1/186 anomalies), in case MDB291
• Long umbilical cord 0.54% (1/186 anomalies), in case MDB291
• Microretrognathia 0.54% (1/186 anomalies), in case MDB258
• Short philtrum 0.54% (1/186 anomalies), in case MDB258
• Sloping forehead 0.54% (1/186 anomalies), in case MDB258
• Neuronal migration anomaly 0.54% (1/186 anomalies), in case MDB258
• Hypogenesis of pyramidal tracts 0.54% (1/186 anomalies), in case MDB258
• Glial heterotopia, multi-focal 0.54% (1/186 anomalies), in case MDB258
• Megacystis 0.54% (1/186 anomalies), in case MDB329
• Dilatation of ureter , bilateral, congenital 0.54% (1/186 anomalies), in case MDB329
• Prominent upper lip 0.54% (1/186 anomalies), in case MDB329
• Short neck 0.54% (1/186 anomalies), in case MDB329
• Cystic hygroma 0.54% (1/186 anomalies), in case MDB329
• Arthrogryposis 0.54% (1/186 anomalies), in case MDB329
• Hydromyelia 0.54% (1/186 anomalies), in case MDB329
• Micromelia, lower limb, unilateral 0.54% (1/186 anomalies), in case MDB329
• Ventricular septal defect, muscular 0.54% (1/186 anomalies), in case MDB329
• Flattened occiput 0.54% (1/186 anomalies), in case MDB68
• Frontal bossing 0.54% (1/186 anomalies), in case MDB68
• Hexadactyly, postaxial 0.54% (1/186 anomalies), in case MDB68
• Vertex aplasia cutis (ACC) 0.54% (1/186 anomalies), in case MDB68
• Polysplenia 0.54% (1/186 anomalies), in case MDB68
• Mongoloid slope of the palpebral fissures 0.54% (1/186 anomalies), in case MDB68
• Rocker-bottom feet 0.54% (1/186 anomalies), in case MDB68
• Cebocephaly 0.54% (1/186 anomalies), in case MDB68
• Nasal hypoplasia 0.54% (1/186 anomalies), in case MDB263
• Absence of first finger, unilateral 0.54% (1/186 anomalies), in case MDB263
• Neck edema 0.54% (1/186 anomalies), in case MDB263
• Exophthalmos, bilateral 0.54% (1/186 anomalies), in case MDB263
• Gothic palate 0.54% (1/186 anomalies), in case MDB263
• Fissure of the upper gingiva, fetal 0.54% (1/186 anomalies), in case MDB263
• Hypoplastic left heart syndrome (HLHS) 0.54% (1/186 anomalies), in case MDB340
• Hypoplasia of ascending aorta 0.54% (1/186 anomalies), in case MDB340
• Hypoplasia of the aortic isthmus 0.54% (1/186 anomalies), in case MDB340
• Defective developement of left ventricle 0.54% (1/186 anomalies), in case MDB340
• Mitral valve stenosis 0.54% (1/186 anomalies), in case MDB340
• Pulmonary artery dilatation, fetal 0.54% (1/186 anomalies), in case MDB340
• Bicornuate uterus 0.54% (1/186 anomalies), in case MDB340
• Pachygyria 0.54% (1/186 anomalies), in case MDB340
• Prominent and pointed nose 0.54% (1/186 anomalies), in case MDB436
• Absence of neuron differentiation in the basal nuclei. 0.54% (1/186 anomalies), in case MDB436
• Prognathism, mandibular 0.54% (1/186 anomalies), in case MDB469
• Large nose, fetal 0.54% (1/186 anomalies), in case MDB469
• Exophthalmos, unilateral 0.54% (1/186 anomalies), in case MDB469
• Recessed forehead 0.54% (1/186 anomalies), in case MDB469
• Small anterior fontanel 0.54% (1/186 anomalies), in case MDB469
• Renal ectopia,crossed 0.54% (1/186 anomalies), in case MDB469
• Renal hypoplasia, unilateral 0.54% (1/186 anomalies), in case MDB469
• Wide space between 1st and 2nd toes, unilateral 0.54% (1/186 anomalies), in case MDB469
• Wide space between 1st and 2nd fingers, unilateral 0.54% (1/186 anomalies), in case MDB469
• Absence of the Septum Pellucidum 0.54% (1/186 anomalies), in case MDB469