Malformations.org

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

• Microcephaly 5.88% (3/51 anomalies), in cases MDB14, MDB291, MDB336
• Corpus callosum agenesis 3.92% (2/51 anomalies), in cases MDB14, MDB291
• Thalamic nuclei centrum medianum fusion 3.92% (2/51 anomalies), in cases MDB14, MDB291
• Neuronal migration anomaly 3.92% (2/51 anomalies), in cases MDB267, MDB336
• Holoprosencephaly, alobar 1.96% (1/51 anomalies), in case MDB14
• Hypogenesis of the Cerebellar Vermis 1.96% (1/51 anomalies), in case MDB14
• Hypotelorisme 1.96% (1/51 anomalies), in case MDB14
• Obstetrician's hand 1.96% (1/51 anomalies), in case MDB14
• Polymicrogyria, focal 1.96% (1/51 anomalies), in case MDB14
• Cleft palate with cleft lip,bilateral, complete 1.96% (1/51 anomalies), in case MDB14
• Communicating hydrocephalus 1.96% (1/51 anomalies), in case MDB267
• Purkinje cell ectopia in the cerebellum 1.96% (1/51 anomalies), in case MDB267
• Subcortical band heterotopia. 1.96% (1/51 anomalies), in case MDB267
• Cortical dysgenesis (CD), diffuse 1.96% (1/51 anomalies), in case MDB267
• Talipes equinovarus, bilateral 1.96% (1/51 anomalies), in case MDB267
• Wide space between 1st and 2nd toes, bilateral 1.96% (1/51 anomalies), in case MDB267
• Lissencephaly, Type II 1.96% (1/51 anomalies), in case MDB267
• Absence of Cajal-Retzius cell 1.96% (1/51 anomalies), in case MDB267
• Hypoplasia of optic nerve, bilateral 1.96% (1/51 anomalies), in case MDB291
• Olfactory bulbs, absence of 1.96% (1/51 anomalies), in case MDB291
• Olfactory nerve, absence of, bilateral 1.96% (1/51 anomalies), in case MDB291
• Holoprosencephaly, lobar 1.96% (1/51 anomalies), in case MDB291
• Arhinencephaly 1.96% (1/51 anomalies), in case MDB291
• Single cerebral ventricule 1.96% (1/51 anomalies), in case MDB291
• Intrauterine growth retardation, symmetric 1.96% (1/51 anomalies), in case MDB291
• Anophthalmos, bilateral 1.96% (1/51 anomalies), in case MDB291
• Arhinia 1.96% (1/51 anomalies), in case MDB291
• Microstomia 1.96% (1/51 anomalies), in case MDB291
• Trigonocephaly 1.96% (1/51 anomalies), in case MDB291
• Micrognathia 1.96% (1/51 anomalies), in case MDB291
• Cyclopia 1.96% (1/51 anomalies), in case MDB291
• Absence of neocortex 1.96% (1/51 anomalies), in case MDB291
• Cerebellar hypoplasia 1.96% (1/51 anomalies), in case MDB291
• Pulmonary hypoplasia 1.96% (1/51 anomalies), in case MDB291
• Placenta hypoplasia 1.96% (1/51 anomalies), in case MDB291
• Long umbilical cord 1.96% (1/51 anomalies), in case MDB291
• Polymicrogyria, diffuse 1.96% (1/51 anomalies), in case MDB336
• Hypertelorism 1.96% (1/51 anomalies), in case MDB336
• Nonimmune hydrops fetalis (NIHF) 1.96% (1/51 anomalies), in case MDB336
• Dysplasia of deep nuclei (olive dysplasia) 1.96% (1/51 anomalies), in case MDB336
• Partial agenesis of the corpus callosum (PACC) 1.96% (1/51 anomalies), in case MDB336
• Brachycephaly 1.96% (1/51 anomalies), in case MDB336
• Rocker-bottom feet 1.96% (1/51 anomalies), in case MDB336
• Hepatomegaly, fetal 1.96% (1/51 anomalies), in case MDB336
• Splenomegaly, congenital 1.96% (1/51 anomalies), in case MDB336
• Renal pelvis dilatation, bilateral 1.96% (1/51 anomalies), in case MDB336