Malformations.org

Synonyms:

• Accessory finger(s)&toe(s)

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

• Facial dysmorphism 4.88% (4/82 anomalies), in cases MDB37, MDB136, MDB427, MDB459
• Hypertelorism 3.66% (3/82 anomalies), in cases MDB20, MDB136, MDB459
• Placenta hypoplasia 3.66% (3/82 anomalies), in cases MDB37, MDB136, MDB434
• Low-set ears 3.66% (3/82 anomalies), in cases MDB136, MDB427, MDB459
• Cleft palate with cleft lip,bilateral, complete 2.44% (2/82 anomalies), in cases MDB37, MDB459
• Pulmonary hypoplasia 2.44% (2/82 anomalies), in cases MDB37, MDB534
• Nephromegaly, bilateral 2.44% (2/82 anomalies), in cases MDB37, MDB459
• Meckel diverticulum 2.44% (2/82 anomalies), in cases MDB37, MDB136
• Coarctation of aorta, 2.44% (2/82 anomalies), in cases MDB136, MDB427
• Defective developement of left ventricle 2.44% (2/82 anomalies), in cases MDB136, MDB534
• Intestinal malrotation 2.44% (2/82 anomalies), in cases MDB136, MDB534
• Multicystic renal dysplasia,bilateral 1.22% (1/82 anomalies), in case MDB20
• Sloping forehead 1.22% (1/82 anomalies), in case MDB20
• Myelomeningocele, lumbosacral 1.22% (1/82 anomalies), in case MDB37
• Flat face 1.22% (1/82 anomalies), in case MDB37
• Hypotelorisme 1.22% (1/82 anomalies), in case MDB37
• Micropenis 1.22% (1/82 anomalies), in case MDB37
• Rachischisis 1.22% (1/82 anomalies), in case MDB37
• Splenomegaly, congenital 1.22% (1/82 anomalies), in case MDB37
• Holoprosencephaly, alobar 1.22% (1/82 anomalies), in case MDB37
• Thalamic nuclei centrum medianum fusion 1.22% (1/82 anomalies), in case MDB37
• Corpus callosum agenesis 1.22% (1/82 anomalies), in case MDB37
• Microtia 1.22% (1/82 anomalies), in case MDB37
• Pulmonary artery dilatation, fetal 1.22% (1/82 anomalies), in case MDB136
• Aortic valve stenosis, congenital 1.22% (1/82 anomalies), in case MDB136
• Right ventricle dilatation 1.22% (1/82 anomalies), in case MDB136
• Right atrium Enlargement 1.22% (1/82 anomalies), in case MDB136
• Retrognathia 1.22% (1/82 anomalies), in case MDB136
• Single transverse palmar crease, unilateral 1.22% (1/82 anomalies), in case MDB136
• Clindodactyly of 5th finger, unilateral 1.22% (1/82 anomalies), in case MDB136
• Intrauterine growth retardation, symmetric 1.22% (1/82 anomalies), in case MDB136
• Dandy-Walker malformation 1.22% (1/82 anomalies), in case MDB427
• Cystic dilatation of the fourth ventricle 1.22% (1/82 anomalies), in case MDB427
• Hypogenesis of the Cerebellar Vermis 1.22% (1/82 anomalies), in case MDB427
• Broad nasal bridge 1.22% (1/82 anomalies), in case MDB427
• Microretrognathia 1.22% (1/82 anomalies), in case MDB427
• Aplasia cutis congenita, scalp 1.22% (1/82 anomalies), in case MDB427
• Anomalous pulmonary veins connection to superior & inferior vena cava 1.22% (1/82 anomalies), in case MDB427
• Hypoplastic left atrium and ventricle 1.22% (1/82 anomalies), in case MDB427
• Hypoplastic right atrium 1.22% (1/82 anomalies), in case MDB427
• Single umblical artery (SUA)-Isolated 1.22% (1/82 anomalies), in case MDB427
• Cyclopia 1.22% (1/82 anomalies), in case MDB434
• Arhinia 1.22% (1/82 anomalies), in case MDB434
• Microstomia 1.22% (1/82 anomalies), in case MDB434
• Neck edema 1.22% (1/82 anomalies), in case MDB434
• Absence of diaphragm, left 1.22% (1/82 anomalies), in case MDB434
• Dextroposition of aorta 1.22% (1/82 anomalies), in case MDB434
• Proboscis 1.22% (1/82 anomalies), in case MDB434
• Holoprosencephaly 1.22% (1/82 anomalies), in case MDB434
• Ventricular septal defect, membranous 1.22% (1/82 anomalies), in case MDB434
• Craniofacial dysmorphism 1.22% (1/82 anomalies), in case MDB434
• Hypospadias, penile 1.22% (1/82 anomalies), in case MDB459
• Adrenal hypoplasia, fetal 1.22% (1/82 anomalies), in case MDB459
• Micromulticystic kidneys 1.22% (1/82 anomalies), in case MDB459
• Short rib polydactyly syndrome, type 1 1.22% (1/82 anomalies), in case MDB534
• Narrow thorax 1.22% (1/82 anomalies), in case MDB534
• Micromelia 1.22% (1/82 anomalies), in case MDB534
• Syndactyly of the toes, complex, bilateral 1.22% (1/82 anomalies), in case MDB534
• Hypoplasia of ascending aorta 1.22% (1/82 anomalies), in case MDB534
• Aortic valve atresia 1.22% (1/82 anomalies), in case MDB534
• Mitral valve stenosis 1.22% (1/82 anomalies), in case MDB534
• Nonimmune hydrops fetalis (NIHF) 1.22% (1/82 anomalies), in case MDB534
• Ascites, fetal 1.22% (1/82 anomalies), in case MDB534
• Large nose, fetal 1.22% (1/82 anomalies), in case MDB534
• Low nasal bridge 1.22% (1/82 anomalies), in case MDB534
• Short neck 1.22% (1/82 anomalies), in case MDB534