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Single umblical artery (SUA)-Isolated

DA: 31

Developmental anomaly information

Definition: Single umbilical artery (SUA) or congenital absence and hypoplasia of umbilical artery is the most common abnormality of the umbilical cord. It is associated with an increased incidence of atresia of hollow organs, renal abnormalities, limb reduction defects and spontaneous abortions. The aetiopathogenesis, although unknown, is attributed to vascular disruption.

Synonyms:

Two- vessel cord

Developmental anomaly parent: (empty)	Topology: (empty)
System: (empty)	Developmental anomaly category: Anomaly of underdevelopment or overdevelopment

Case records MDB9, MDB30, MDB51, MDB56, MDB70, MDB105, MDB115, MDB138, MDB155, MDB173, MDB179, MDB195, MDB209, MDB215, MDB246, MDB247, MDB276, MDB278, MDB296, MDB325, MDB333, MDB358, MDB359, MDB361, MDB53, MDB373, MDB382, MDB391, MDB418, MDB420, MDB427, MDB448, MDB464, MDB465, MDB478, MDB487, MDB492, MDB496, MDB501, MDB521, MDB532, MDB541, MDB262, MDB99, MDB322, MDB388, MDB428

Links

Humpath: 13297

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

() in cases MDB, MDB, MDB, MDB, MDB

Associated genes in profile

Associated genes in malformative diseases

Associated chromosomal diseases

Associated signaling pathways

Associated developmental anomalies

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

Pulmonary hypoplasia 3.79% (18/475 anomalies), in cases MDB9, MDB30, MDB56, MDB155, MDB209, MDB246, MDB325, MDB333, MDB359, MDB382, MDB391, MDB465, MDB478, MDB487, MDB496, MDB521, MDB322, MDB388
Facial dysmorphism 3.37% (16/475 anomalies), in cases MDB9, MDB30, MDB56, MDB70, MDB105, MDB115, MDB215, MDB278, MDB358, MDB359, MDB53, MDB391, MDB418, MDB427, MDB448, MDB487
Intrauterine growth retardation, symmetric 3.37% (16/475 anomalies), in cases MDB105, MDB115, MDB173, MDB215, MDB246, MDB278, MDB358, MDB359, MDB53, MDB391, MDB418, MDB420, MDB465, MDB99, MDB322, MDB388
Placenta hypoplasia 2.32% (11/475 anomalies), in cases MDB56, MDB209, MDB215, MDB278, MDB333, MDB358, MDB359, MDB382, MDB492, MDB496, MDB322
Talipes equinovarus, bilateral 2.11% (10/475 anomalies), in cases MDB115, MDB209, MDB215, MDB246, MDB333, MDB391, MDB418, MDB464, MDB322, MDB428
Low-set ears 1.89% (9/475 anomalies), in cases MDB9, MDB70, MDB209, MDB215, MDB325, MDB359, MDB53, MDB427, MDB428
Imperforate Anus 1.89% (9/475 anomalies), in cases MDB115, MDB179, MDB209, MDB246, MDB325, MDB382, MDB492, MDB521, MDB262
Omphalocele 1.47% (7/475 anomalies), in cases MDB9, MDB70, MDB155, MDB325, MDB359, MDB420, MDB487
Coarctation of aorta, 1.47% (7/475 anomalies), in cases MDB105, MDB333, MDB53, MDB373, MDB391, MDB427, MDB262
Hypertelorism 1.26% (6/475 anomalies), in cases MDB105, MDB138, MDB215, MDB358, MDB448, MDB322
Microretrognathia 1.26% (6/475 anomalies), in cases MDB105, MDB325, MDB333, MDB427, MDB478, MDB322
Renal agenesis, unilateral 1.26% (6/475 anomalies), in cases MDB138, MDB325, MDB358, MDB382, MDB501, MDB521
Lobulated, fused and horseshoe kidney 1.26% (6/475 anomalies), in cases MDB359, MDB53, MDB391, MDB487, MDB541, MDB262
Micrognathia 1.05% (5/475 anomalies), in cases MDB9, MDB209, MDB448, MDB501, MDB262
Short neck 1.05% (5/475 anomalies), in cases MDB215, MDB487, MDB496, MDB322, MDB428
Multicystic renal dysplasia,bilateral 1.05% (5/475 anomalies), in cases MDB215, MDB278, MDB418, MDB496, MDB262
Retrognathia 1.05% (5/475 anomalies), in cases MDB358, MDB359, MDB391, MDB487, MDB262
Posteriorly inclined and low-positioned ears 1.05% (5/475 anomalies), in cases MDB418, MDB487, MDB496, MDB501, MDB532
Clindodactyly of 5th finger, bilateral 0.84% (4/475 anomalies), in cases MDB56, MDB215, MDB391, MDB487
Broad nasal bridge 0.84% (4/475 anomalies), in cases MDB105, MDB215, MDB427, MDB322
Overlapping fingers 0.84% (4/475 anomalies), in cases MDB105, MDB155, MDB179, MDB322
Crossed fused renal ectopia 0.84% (4/475 anomalies), in cases MDB115, MDB173, MDB532, MDB262
Gothic palate 0.84% (4/475 anomalies), in cases MDB155, MDB478, MDB496, MDB322
Transverse palmar crease, bilateral 0.63% (3/475 anomalies), in cases MDB30, MDB448, MDB99
Aberrant right subclavian artery 0.63% (3/475 anomalies), in cases MDB30, MDB155, MDB209
Right ventricular hypoplasia 0.63% (3/475 anomalies), in cases MDB105, MDB246, MDB296
Persistent left superior vena cava 0.63% (3/475 anomalies), in cases MDB105, MDB209, MDB418
Right bilobate lung 0.63% (3/475 anomalies), in cases MDB105, MDB215, MDB521
Meckel diverticulum 0.63% (3/475 anomalies), in cases MDB138, MDB173, MDB179
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.63% (3/475 anomalies), in cases MDB155, MDB173, MDB179
Hydroureter, unilateral 0.63% (3/475 anomalies), in cases MDB179, MDB501, MDB262
Persistent truncus arteriosus 0.63% (3/475 anomalies), in cases MDB195, MDB247, MDB532
Bladder hypoplasia 0.63% (3/475 anomalies), in cases MDB209, MDB278, MDB418
Pulmonary artery hypoplasia 0.63% (3/475 anomalies), in cases MDB246, MDB296, MDB418
Trilobate lung, bilateral 0.63% (3/475 anomalies), in cases MDB247, MDB420, MDB487
Polydactyly of the hand, preaxial 0.63% (3/475 anomalies), in cases MDB247, MDB322, MDB322
Hypogenesis of the Cerebellar Vermis 0.63% (3/475 anomalies), in cases MDB278, MDB359, MDB427
Narrow thorax 0.63% (3/475 anomalies), in cases MDB358, MDB464, MDB487
Adrenal hypoplasia, fetal 0.63% (3/475 anomalies), in cases MDB358, MDB465, MDB487
Ventricular septal defect, muscular 0.63% (3/475 anomalies), in cases MDB53, MDB391, MDB418
Large anterior fontanelle 0.63% (3/475 anomalies), in cases MDB53, MDB487, MDB428
Prominent and pointed nose 0.63% (3/475 anomalies), in cases MDB391, MDB487, MDB428
Ventricular septal defect, membranous 0.63% (3/475 anomalies), in cases MDB420, MDB465, MDB388
Neck edema 0.63% (3/475 anomalies), in cases MDB496, MDB532, MDB322
Scoliosis, congenital 0.42% (2/475 anomalies), in cases MDB9, MDB105
Macroglossia 0.42% (2/475 anomalies), in cases MDB30, MDB496
Wide space between 1st and 2nd toes, unilateral 0.42% (2/475 anomalies), in cases MDB30, MDB322
Pleural effusion, fetal 0.42% (2/475 anomalies), in cases MDB30, MDB333
Defective developement of left ventricle 0.42% (2/475 anomalies), in cases MDB51, MDB195
Aortic valve stenosis, congenital 0.42% (2/475 anomalies), in cases MDB51, MDB105
Hypoplasia of ascending aorta 0.42% (2/475 anomalies), in cases MDB51, MDB105
Macrocephaly 0.42% (2/475 anomalies), in cases MDB70, MDB358
Retroplacental hemorrhage 0.42% (2/475 anomalies), in cases MDB70, MDB195
Sloping forehead 0.42% (2/475 anomalies), in cases MDB105, MDB322
Gracile ribs 0.42% (2/475 anomalies), in cases MDB105, MDB322
Cubital pterygium, bilateral 0.42% (2/475 anomalies), in cases MDB105, MDB325
Aortic isthmus stenosis 0.42% (2/475 anomalies), in cases MDB105, MDB521
Rocker-bottom feet 0.42% (2/475 anomalies), in cases MDB105, MDB532
Right atrium Enlargement 0.42% (2/475 anomalies), in cases MDB105, MDB246
Right aortic arch 0.42% (2/475 anomalies), in cases MDB138, MDB418
Ureter agenesis, unilateral 0.42% (2/475 anomalies), in cases MDB138, MDB501
Polydactyly,of the hand, postaxial 0.42% (2/475 anomalies), in cases MDB155, MDB501
Split-hand/split-foot malformation (SHFM) 0.42% (2/475 anomalies), in cases MDB173, MDB501
Hydronephrosis, congenital, unilateral 0.42% (2/475 anomalies), in cases MDB179, MDB262
Hypospadias, penile 0.42% (2/475 anomalies), in cases MDB179, MDB262
Flattened nose 0.42% (2/475 anomalies), in cases MDB209, MDB325
Potter deformity sequence 0.42% (2/475 anomalies), in cases MDB209, MDB325
Toe hypoplasia, first, bilateral 0.42% (2/475 anomalies), in cases MDB246, MDB448
Dandy-Walker malformation 0.42% (2/475 anomalies), in cases MDB276, MDB427
Hydrocephalus, Non-communicating 0.42% (2/475 anomalies), in cases MDB276, MDB541
Nephromegaly, bilateral 0.42% (2/475 anomalies), in cases MDB278, MDB478
Camptodactyly, unilateral 0.42% (2/475 anomalies), in cases MDB278, MDB496
Nonimmune hydrops fetalis (NIHF) 0.42% (2/475 anomalies), in cases MDB333, MDB373
Splenomegaly, congenital 0.42% (2/475 anomalies), in cases MDB333, MDB478
Exophthalmos, bilateral 0.42% (2/475 anomalies), in cases MDB358, MDB496
Ureteral duplication, complete, unilateral 0.42% (2/475 anomalies), in cases MDB358, MDB487
Triangular face 0.42% (2/475 anomalies), in cases MDB359, MDB53
Giant omphalocele 0.42% (2/475 anomalies), in cases MDB53, MDB492
Cystic hygroma 0.42% (2/475 anomalies), in cases MDB373, MDB391
Dextrocardia, isolated 0.42% (2/475 anomalies), in cases MDB391, MDB418
Preauricular hamartoma 0.42% (2/475 anomalies), in cases MDB391, MDB391
Unicorn Uterus 0.42% (2/475 anomalies), in cases MDB418, MDB501
Anencephaly 0.42% (2/475 anomalies), in cases MDB464, MDB496
Anencephaly facies 0.42% (2/475 anomalies), in cases MDB464, MDB496
Hypertrophy of the Thymus 0.42% (2/475 anomalies), in cases MDB464, MDB478
Long philtrum 0.42% (2/475 anomalies), in cases MDB478, MDB322
Pulmonary lobation anomalies 0.42% (2/475 anomalies), in cases MDB478, MDB262
Rectovesical fistula 0.42% (2/475 anomalies), in cases MDB521, MDB262
Neuronal migration anomaly 0.42% (2/475 anomalies), in cases MDB541, MDB322
Cerebral ventriculomegaly 0.42% (2/475 anomalies), in cases MDB541, MDB541
Polysplenia 0.42% (2/475 anomalies), in cases MDB262, MDB322
Ascites, fetal 0.21% (1/475 anomalies), in case MDB9
Low nasal bridge 0.21% (1/475 anomalies), in case MDB9
Varus deviation of fingers 0.21% (1/475 anomalies), in case MDB9
Mitral valve stenosis 0.21% (1/475 anomalies), in case MDB51
Endocardial fibroelastosis 0.21% (1/475 anomalies), in case MDB51
Diaphragmatic hernia, congenital 0.21% (1/475 anomalies), in case MDB56
cutaneous edema, fetal 0.21% (1/475 anomalies), in case MDB56
Absence of one paire the rib 0.21% (1/475 anomalies), in case MDB56
Frontal bossing 0.21% (1/475 anomalies), in case MDB70
Lymphedema of the neck 0.21% (1/475 anomalies), in case MDB70
Axillary pterygia,unilateral 0.21% (1/475 anomalies), in case MDB105
Pulmonary artery dilatation, fetal 0.21% (1/475 anomalies), in case MDB105
Platyspondyly 0.21% (1/475 anomalies), in case MDB105
snub-nosed 0.21% (1/475 anomalies), in case MDB105
Polyhydramnios 0.21% (1/475 anomalies), in case MDB105
dextro-Transposition of the great arteries 0.21% (1/475 anomalies), in case MDB105
Cleft palate, bilateral, complete 0.21% (1/475 anomalies), in case MDB105
Thumb agenesis, unilateral 0.21% (1/475 anomalies), in case MDB115
Constriction Ring Deformity of the upper limbs 0.21% (1/475 anomalies), in case MDB115
Encephalocele, parietal 0.21% (1/475 anomalies), in case MDB115
Bifid rib 0.21% (1/475 anomalies), in case MDB138
Abnormal vertebral segmentation 0.21% (1/475 anomalies), in case MDB138
Aberrant left subclavian artery 0.21% (1/475 anomalies), in case MDB138
Supernumerary ribs 0.21% (1/475 anomalies), in case MDB138
Abnormal formation of the cerebellar gyri 0.21% (1/475 anomalies), in case MDB155
Badly-hemmed ears 0.21% (1/475 anomalies), in case MDB155
Purkinje cell ectopia in the cerebellum 0.21% (1/475 anomalies), in case MDB155
Olfactory nerve, absence of, unilateral 0.21% (1/475 anomalies), in case MDB155
Olfactory nerve hypoplasia,unilateral 0.21% (1/475 anomalies), in case MDB155
Hypoplasia of the humerus, unilateral 0.21% (1/475 anomalies), in case MDB173
Ovarian hypoplasia, unilateral 0.21% (1/475 anomalies), in case MDB173
fallopian tube dysgenesis 0.21% (1/475 anomalies), in case MDB173
genital ambiguity 0.21% (1/475 anomalies), in case MDB173
Uterus agenesis 0.21% (1/475 anomalies), in case MDB173
Toe hypoplasia, first, unilateral 0.21% (1/475 anomalies), in case MDB179
Absence of six tarsal bones, unilateral 0.21% (1/475 anomalies), in case MDB179
Proximal Focal Femoral Deficiency 0.21% (1/475 anomalies), in case MDB179
Fibular Hemimelia: 0.21% (1/475 anomalies), in case MDB179
Metatarsus adductus 0.21% (1/475 anomalies), in case MDB179
Placenta circumvallata 0.21% (1/475 anomalies), in case MDB179
Marginal subchorionic hematoma 0.21% (1/475 anomalies), in case MDB179
Mitral valve atresia 0.21% (1/475 anomalies), in case MDB195
Renal agenesis, bilateral 0.21% (1/475 anomalies), in case MDB209
Potter's facies 0.21% (1/475 anomalies), in case MDB209
Ureter agenesis, bilateral 0.21% (1/475 anomalies), in case MDB209
Prostate hypoplasia 0.21% (1/475 anomalies), in case MDB209
Pericardial effusion 0.21% (1/475 anomalies), in case MDB209
Micromelia 0.21% (1/475 anomalies), in case MDB215
Cleft palate, median posterior 0.21% (1/475 anomalies), in case MDB215
Microphthalmia 0.21% (1/475 anomalies), in case MDB215
Unilobate lung, unilateral 0.21% (1/475 anomalies), in case MDB215
Shortening (micromelia) of upper limb(s) 0.21% (1/475 anomalies), in case MDB246
Amelia of the upper limb, unilateral 0.21% (1/475 anomalies), in case MDB246
Renal hypoplasia 0.21% (1/475 anomalies), in case MDB246
Dysplasia of hip, unilateral, congenital 0.21% (1/475 anomalies), in case MDB246
Scrotal hypoplasia 0.21% (1/475 anomalies), in case MDB246
Preauricular fistula, congenital (PAFC) 0.21% (1/475 anomalies), in case MDB247
Asplenia 0.21% (1/475 anomalies), in case MDB247
Dextroposition of stomach and pancreas 0.21% (1/475 anomalies), in case MDB247
Gastroschisis 0.21% (1/475 anomalies), in case MDB276
Spina bifida occulta, lombosacral 0.21% (1/475 anomalies), in case MDB278
Limbs hypoplasia 0.21% (1/475 anomalies), in case MDB278
Syndactyly of the toes, unilateral 0.21% (1/475 anomalies), in case MDB278
Long umbilical cord 0.21% (1/475 anomalies), in case MDB278
Pulmonary valve atresia 0.21% (1/475 anomalies), in case MDB296
Left ventricular hypertrophy, 0.21% (1/475 anomalies), in case MDB296
Flexion contracture of lower limbs 0.21% (1/475 anomalies), in case MDB325
Popliteal pterygium 0.21% (1/475 anomalies), in case MDB325
Scoliosis, thoracic, left 0.21% (1/475 anomalies), in case MDB325
Multicystic renal dysplasia, unilateral 0.21% (1/475 anomalies), in case MDB325
Micromelia, lower limbs 0.21% (1/475 anomalies), in case MDB325
flexion contracture of the forearm 0.21% (1/475 anomalies), in case MDB325
Rib fusions 0.21% (1/475 anomalies), in case MDB325
Large ear, fetal 0.21% (1/475 anomalies), in case MDB325
Dorsiflexion of foot, unilateral 0.21% (1/475 anomalies), in case MDB325
Scalloping of the frontal bones 0.21% (1/475 anomalies), in case MDB325
Talipes equinovarus,unilateral 0.21% (1/475 anomalies), in case MDB325
Triploidy, Maternal, nonmolar (triploidy by digyny) 0.21% (1/475 anomalies), in case MDB358
Aglossia 0.21% (1/475 anomalies), in case MDB358
Syndactyly of the fingers, complex, bilateral 0.21% (1/475 anomalies), in case MDB358
Unilobate lung, bilateral 0.21% (1/475 anomalies), in case MDB358
Dermoid cyst of the ovary 0.21% (1/475 anomalies), in case MDB358
Malformed ear 0.21% (1/475 anomalies), in case MDB359
Hypoplastic left heart syndrome (HLHS) 0.21% (1/475 anomalies), in case MDB361
hypoplasia of the rib 0.21% (1/475 anomalies), in case MDB53
Renal pelvis dilatation, unilateral 0.21% (1/475 anomalies), in case MDB53
Radial ray agenesis, unilateral 0.21% (1/475 anomalies), in case MDB53
Syndactyly, simple (webbed), fingers 0.21% (1/475 anomalies), in case MDB53
Clindodactyly of 5th finger, unilateral 0.21% (1/475 anomalies), in case MDB53
Laparoschisis 0.21% (1/475 anomalies), in case MDB382
Anorchia, unilateral 0.21% (1/475 anomalies), in case MDB382
Megacystis 0.21% (1/475 anomalies), in case MDB382
Hypodactyly, hand, unilateral 0.21% (1/475 anomalies), in case MDB382
overlapping skull bones 0.21% (1/475 anomalies), in case MDB382
Anotia 0.21% (1/475 anomalies), in case MDB391
Absence of diaphragm, left 0.21% (1/475 anomalies), in case MDB391
Intestinal malrotation 0.21% (1/475 anomalies), in case MDB391
Pterygium colli 0.21% (1/475 anomalies), in case MDB391
Pectus excavatum 0.21% (1/475 anomalies), in case MDB391
Ureter hypoplasia 0.21% (1/475 anomalies), in case MDB418
Fallopian tube, absence of 0.21% (1/475 anomalies), in case MDB418
Cleft palate with cleft lip,bilateral, complete 0.21% (1/475 anomalies), in case MDB418
Cystic dilatation of the fourth ventricle 0.21% (1/475 anomalies), in case MDB427
Aplasia cutis congenita, scalp 0.21% (1/475 anomalies), in case MDB427
Polydactyly of both fingers & toes, postaxial 0.21% (1/475 anomalies), in case MDB427
Anomalous pulmonary veins connection to superior & inferior vena cava 0.21% (1/475 anomalies), in case MDB427
Hypoplastic left atrium and ventricle 0.21% (1/475 anomalies), in case MDB427
Hypoplastic right atrium 0.21% (1/475 anomalies), in case MDB427
Acrocephaly 0.21% (1/475 anomalies), in case MDB448
Large nose, fetal 0.21% (1/475 anomalies), in case MDB448
Overlapping toes 0.21% (1/475 anomalies), in case MDB448
Placenta villous fibrosis 0.21% (1/475 anomalies), in case MDB448
Encephalocele, occipital 0.21% (1/475 anomalies), in case MDB464
Googly eyes 0.21% (1/475 anomalies), in case MDB464
Eventration of the diaphragm 0.21% (1/475 anomalies), in case MDB464
Bulbous nose 0.21% (1/475 anomalies), in case MDB478
Periventricular Leukomalacia (PVL) 0.21% (1/475 anomalies), in case MDB478
Tetralogy of Fallot 0.21% (1/475 anomalies), in case MDB492
Renal ectopia,crossed 0.21% (1/475 anomalies), in case MDB492
Mandibulofacial dysostosis 0.21% (1/475 anomalies), in case MDB501
Polydactyly of the foot 0.21% (1/475 anomalies), in case MDB501
Acro–renal–mandibular syndrome 0.21% (1/475 anomalies), in case MDB501
Megarectum 0.21% (1/475 anomalies), in case MDB521
Esophageal Atresia with proximal TEF (tracheoesophageal fistula)Type B 0.21% (1/475 anomalies), in case MDB521
Left vertebral artery aberration 0.21% (1/475 anomalies), in case MDB521
Dysplasia of deep nuclei (olive dysplasia) 0.21% (1/475 anomalies), in case MDB541
Subcortical band heterotopia. 0.21% (1/475 anomalies), in case MDB541
Forking form type of the stenosis of aqueduct of Sylvius 0.21% (1/475 anomalies), in case MDB541
Duodenal atresia and stenosis, congenital 0.21% (1/475 anomalies), in case MDB262
Cloacal dysgenesis sequence (CDS) 0.21% (1/475 anomalies), in case MDB262
Renal hypoplasia, unilateral 0.21% (1/475 anomalies), in case MDB262
Placental hypermaturity 0.21% (1/475 anomalies), in case MDB262
Microcephaly 0.21% (1/475 anomalies), in case MDB322
Camptodactyly, bilateral 0.21% (1/475 anomalies), in case MDB322
Syndactyly of the feet , simple (webbed), unilateral 0.21% (1/475 anomalies), in case MDB322
Lower limb hyperextension, Fetal 0.21% (1/475 anomalies), in case MDB322
Scoliosis, dextroconvex, thoracic 0.21% (1/475 anomalies), in case MDB322
Cortical dysgenesis (CD), diffuse 0.21% (1/475 anomalies), in case MDB322
Hydrocephalus 0.21% (1/475 anomalies), in case MDB322
Absence of neuron differentiation in the basal nuclei. 0.21% (1/475 anomalies), in case MDB322
Flexion contracture of the fingers 0.21% (1/475 anomalies), in case MDB322
Small round skull 0.21% (1/475 anomalies), in case MDB322
Renal pelvis dilatation, bilateral 0.21% (1/475 anomalies), in case MDB388
Dilatation of ureter , bilateral, congenital 0.21% (1/475 anomalies), in case MDB388
Brachydactyly of the toes 0.21% (1/475 anomalies), in case MDB428
Hepatomegaly, fetal 0.21% (1/475 anomalies), in case MDB428

Terminology and coding

References

No reference related to Single umblical artery (SUA)-Isolated is available at the moment.

Last modified: 2008-12-05 14:58:25 by farideh

Created: 2008-02-18 00:00:00 by phsaw

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