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Neck edema

DA: 588

Developmental anomaly information

Definition: Interstitial oedema in the neck region,associated with Trisomy 21 and all other major chromosomal abnormalities.

Synonyms:

nuchal edema

Developmental anomaly parent: (empty)	Topology: Human body > Head and neck > Neck
System: integument & skin	Developmental anomaly category: Deformation

Case records MDB8, MDB17, MDB29, MDB69, MDB92, MDB94, MDB109, MDB121, MDB149, MDB38, MDB198, MDB200, MDB227, MDB279, MDB321, MDB322, MDB367, MDB404, MDB419, MDB434, MDB443, MDB455, MDB470, MDB476, MDB496, MDB506, MDB514, MDB520, MDB523, MDB532, MDB543, MDB203, MDB292, MDB263, MDB310, MDB324, MDB368

Links

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

() in cases 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 :

Low-set ears 4.56% (17/373 anomalies), in cases MDB17, MDB29, MDB69, MDB109, MDB198, MDB227, MDB321, MDB404, MDB419, MDB443, MDB470, MDB476, MDB506, MDB520, MDB543, MDB292, MDB310
Facial dysmorphism 4.02% (15/373 anomalies), in cases MDB17, MDB29, MDB109, MDB198, MDB200, MDB227, MDB279, MDB321, MDB367, MDB443, MDB470, MDB506, MDB520, MDB543, MDB263
Pulmonary hypoplasia 3.22% (12/373 anomalies), in cases MDB29, MDB69, MDB109, MDB149, MDB200, MDB227, MDB322, MDB367, MDB404, MDB443, MDB496, MDB324
Placenta hypoplasia 3.22% (12/373 anomalies), in cases MDB29, MDB200, MDB321, MDB322, MDB419, MDB434, MDB496, MDB520, MDB523, MDB543, MDB263, MDB310
Hypertelorism 2.68% (10/373 anomalies), in cases MDB69, MDB94, MDB198, MDB227, MDB321, MDB322, MDB367, MDB514, MDB520, MDB368
Short neck 2.41% (9/373 anomalies), in cases MDB38, MDB322, MDB367, MDB470, MDB476, MDB496, MDB506, MDB514, MDB368
Intrauterine growth retardation, symmetric 2.41% (9/373 anomalies), in cases MDB321, MDB322, MDB367, MDB404, MDB476, MDB520, MDB263, MDB310, MDB368
Macroglossia 2.14% (8/373 anomalies), in cases MDB17, MDB121, MDB149, MDB38, MDB200, MDB227, MDB496, MDB514
Clindodactyly of 5th finger, bilateral 1.88% (7/373 anomalies), in cases MDB69, MDB149, MDB200, MDB279, MDB514, MDB324, MDB368
Retrognathia 1.88% (7/373 anomalies), in cases MDB279, MDB367, MDB470, MDB476, MDB506, MDB543, MDB368
Micrognathia 1.61% (6/373 anomalies), in cases MDB17, MDB200, MDB404, MDB263, MDB310, MDB324
Low nasal bridge 1.61% (6/373 anomalies), in cases MDB69, MDB443, MDB470, MDB292, MDB324, MDB368
Sloping forehead 1.61% (6/373 anomalies), in cases MDB69, MDB198, MDB200, MDB279, MDB322, MDB324
Ventricular septal defect, membranous 1.61% (6/373 anomalies), in cases MDB109, MDB404, MDB434, MDB470, MDB506, MDB310
Talipes equinovarus, bilateral 1.34% (5/373 anomalies), in cases MDB29, MDB322, MDB292, MDB310, MDB324
Microretrognathia 1.34% (5/373 anomalies), in cases MDB109, MDB322, MDB520, MDB523, MDB292
Broad nasal bridge 1.34% (5/373 anomalies), in cases MDB149, MDB198, MDB321, MDB322, MDB520
Adrenal hypoplasia, fetal 1.34% (5/373 anomalies), in cases MDB367, MDB404, MDB514, MDB520, MDB203
Corpus callosum agenesis 1.07% (4/373 anomalies), in cases MDB8, MDB443, MDB514, MDB263
Microcephaly 1.07% (4/373 anomalies), in cases MDB17, MDB38, MDB322, MDB263
Foot edema 1.07% (4/373 anomalies), in cases MDB29, MDB514, MDB520, MDB523
Hypogenesis of the Cerebellar Vermis 1.07% (4/373 anomalies), in cases MDB69, MDB443, MDB514, MDB310
Transverse palmar crease, bilateral 1.07% (4/373 anomalies), in cases MDB121, MDB227, MDB443, MDB368
Mongoloid slope of the palpebral fissures 1.07% (4/373 anomalies), in cases MDB149, MDB200, MDB227, MDB419
Wide space between 1st and 2nd toes, bilateral 1.07% (4/373 anomalies), in cases MDB149, MDB279, MDB367, MDB470
Communicating hydrocephalus 0.8% (3/373 anomalies), in cases MDB17, MDB38, MDB443
Long philtrum 0.8% (3/373 anomalies), in cases MDB29, MDB322, MDB324
Cerebral ventriculomegaly 0.8% (3/373 anomalies), in cases MDB69, MDB38, MDB520
Nasal hypoplasia 0.8% (3/373 anomalies), in cases MDB69, MDB200, MDB263
Gracile ribs 0.8% (3/373 anomalies), in cases MDB69, MDB109, MDB322
Single transverse palmar crease, unilateral 0.8% (3/373 anomalies), in cases MDB92, MDB38, MDB321
Patent Foramen Ovale 0.8% (3/373 anomalies), in cases MDB109, MDB121, MDB149
Gothic palate 0.8% (3/373 anomalies), in cases MDB322, MDB496, MDB263
Single umblical artery (SUA)-Isolated 0.8% (3/373 anomalies), in cases MDB322, MDB496, MDB532
Flattened nose 0.8% (3/373 anomalies), in cases MDB455, MDB263, MDB324
Large anterior fontanelle 0.8% (3/373 anomalies), in cases MDB470, MDB476, MDB543
Posteriorly inclined and low-positioned ears 0.8% (3/373 anomalies), in cases MDB496, MDB532, MDB324
Retroplacental hemorrhage 0.8% (3/373 anomalies), in cases MDB543, MDB324, MDB368
Toe hypoplasia, first, bilateral 0.8% (3/373 anomalies), in cases MDB263, MDB310, MDB368
Multicystic renal dysplasia,bilateral 0.54% (2/373 anomalies), in cases MDB29, MDB496
Epicanthus 0.54% (2/373 anomalies), in cases MDB29, MDB200
Syndactyly, simple (webbed), fingers 0.54% (2/373 anomalies), in cases MDB69, MDB94
Fingers amputation 0.54% (2/373 anomalies), in cases MDB69, MDB94
Holoprosencephaly 0.54% (2/373 anomalies), in cases MDB69, MDB434
Syndactyly of the toes, complex, bilateral 0.54% (2/373 anomalies), in cases MDB69, MDB94
Toes amputation 0.54% (2/373 anomalies), in cases MDB69, MDB94
Pterygium colli 0.54% (2/373 anomalies), in cases MDB69, MDB321
Renal pelvis dilatation, unilateral 0.54% (2/373 anomalies), in cases MDB92, MDB321
Omphalocele 0.54% (2/373 anomalies), in cases MDB94, MDB109
Right bilobate lung 0.54% (2/373 anomalies), in cases MDB94, MDB109
Ascites, fetal 0.54% (2/373 anomalies), in cases MDB109, MDB324
Hexadactyly, postaxial 0.54% (2/373 anomalies), in cases MDB109, MDB321
Dilatation of the ascending aorta, congenital 0.54% (2/373 anomalies), in cases MDB149, MDB367
Renal pelvis dilatation, bilateral 0.54% (2/373 anomalies), in cases MDB198, MDB324
Polydactyly of the hand, preaxial 0.54% (2/373 anomalies), in cases MDB322, MDB322
Syndactyly of the feet , simple (webbed), unilateral 0.54% (2/373 anomalies), in cases MDB322, MDB310
Bladder hypoplasia 0.54% (2/373 anomalies), in cases MDB455, MDB310
Cerebellar hypoplasia 0.54% (2/373 anomalies), in cases MDB455, MDB310
Exophthalmos, bilateral 0.54% (2/373 anomalies), in cases MDB496, MDB263
Arthrogryposis 0.54% (2/373 anomalies), in cases MDB520, MDB543
Cleft palate, bilateral 0.27% (1/373 anomalies), in case MDB8
Pectus excavatum 0.27% (1/373 anomalies), in case MDB8
Giant omphalocele 0.27% (1/373 anomalies), in case MDB29
Axillary pterygia,unilateral 0.27% (1/373 anomalies), in case MDB29
Tridactyly, unilateral 0.27% (1/373 anomalies), in case MDB29
vertebral bones and gracile ribs with multiple abnormalities 0.27% (1/373 anomalies), in case MDB29
Dandy-Walker malformation 0.27% (1/373 anomalies), in case MDB69
Cleft lip, unilateral 0.27% (1/373 anomalies), in case MDB69
Macrocephaly 0.27% (1/373 anomalies), in case MDB69
Constriction Ring Deformity of the upper limbs 0.27% (1/373 anomalies), in case MDB69
Constriction Ring Deformity of the lower limbs 0.27% (1/373 anomalies), in case MDB69
Ring constriction deformity of the toes 0.27% (1/373 anomalies), in case MDB69
Nasal asymetria 0.27% (1/373 anomalies), in case MDB69
Bowing of femur, congenital 0.27% (1/373 anomalies), in case MDB69
Cubital pterygium, bilateral 0.27% (1/373 anomalies), in case MDB94
Anophthalmos, bilateral 0.27% (1/373 anomalies), in case MDB94
Transverse amputation of limb 0.27% (1/373 anomalies), in case MDB94
Cleft palate with cleft lip,bilateral, complete 0.27% (1/373 anomalies), in case MDB94
overlapping skull bones 0.27% (1/373 anomalies), in case MDB94
Thorax deformation,fetal 0.27% (1/373 anomalies), in case MDB94
Open bite mouth, fetal 0.27% (1/373 anomalies), in case MDB94
Right atrium Enlargement 0.27% (1/373 anomalies), in case MDB109
Nonimmune hydrops fetalis (NIHF) 0.27% (1/373 anomalies), in case MDB109
Cleft palate with cleft lip (CLP), median 0.27% (1/373 anomalies), in case MDB109
Nephromegaly, bilateral 0.27% (1/373 anomalies), in case MDB109
Thymic hypoplasia 0.27% (1/373 anomalies), in case MDB109
Splenomegaly, congenital 0.27% (1/373 anomalies), in case MDB109
Right ventricle dilatation 0.27% (1/373 anomalies), in case MDB109
Tricuspid valve dysplasia 0.27% (1/373 anomalies), in case MDB109
Mitral valve stenosis 0.27% (1/373 anomalies), in case MDB121
Atrioventricular - channel 0.27% (1/373 anomalies), in case MDB121
Duodenal atresia and stenosis, congenital 0.27% (1/373 anomalies), in case MDB121
Tetralogy of Fallot 0.27% (1/373 anomalies), in case MDB149
Ventricular septal defect, muscular 0.27% (1/373 anomalies), in case MDB149
Pulmonary artery hypoplasia 0.27% (1/373 anomalies), in case MDB149
Persistent Ductus arteriosus 0.27% (1/373 anomalies), in case MDB149
Bicuspid pulmonary valve 0.27% (1/373 anomalies), in case MDB149
Short philtrum 0.27% (1/373 anomalies), in case MDB198
Recessed forehead 0.27% (1/373 anomalies), in case MDB200
Flat face 0.27% (1/373 anomalies), in case MDB227
Flattened occiput 0.27% (1/373 anomalies), in case MDB227
Absence of one paire the rib 0.27% (1/373 anomalies), in case MDB227
Hepatomegaly, fetal 0.27% (1/373 anomalies), in case MDB279
Overlapping fingers 0.27% (1/373 anomalies), in case MDB322
Camptodactyly, bilateral 0.27% (1/373 anomalies), in case MDB322
Lower limb hyperextension, Fetal 0.27% (1/373 anomalies), in case MDB322
Polysplenia 0.27% (1/373 anomalies), in case MDB322
Wide space between 1st and 2nd toes, unilateral 0.27% (1/373 anomalies), in case MDB322
Scoliosis, dextroconvex, thoracic 0.27% (1/373 anomalies), in case MDB322
Neuronal migration anomaly 0.27% (1/373 anomalies), in case MDB322
Cortical dysgenesis (CD), diffuse 0.27% (1/373 anomalies), in case MDB322
Hydrocephalus 0.27% (1/373 anomalies), in case MDB322
Absence of neuron differentiation in the basal nuclei. 0.27% (1/373 anomalies), in case MDB322
Flexion contracture of the fingers 0.27% (1/373 anomalies), in case MDB322
Small round skull 0.27% (1/373 anomalies), in case MDB322
Diaphragmatic hernia,unilateral 0.27% (1/373 anomalies), in case MDB367
Dextrocardia, isolated 0.27% (1/373 anomalies), in case MDB367
Coarctation of aorta, 0.27% (1/373 anomalies), in case MDB367
Clindodactyly of 5th finger, unilateral 0.27% (1/373 anomalies), in case MDB367
Aberrant right subclavian artery 0.27% (1/373 anomalies), in case MDB404
left carotid artery, aberrant 0.27% (1/373 anomalies), in case MDB404
Cyclopia 0.27% (1/373 anomalies), in case MDB434
Arhinia 0.27% (1/373 anomalies), in case MDB434
Microstomia 0.27% (1/373 anomalies), in case MDB434
Polydactyly of both fingers & toes, postaxial 0.27% (1/373 anomalies), in case MDB434
Absence of diaphragm, left 0.27% (1/373 anomalies), in case MDB434
Dextroposition of aorta 0.27% (1/373 anomalies), in case MDB434
Proboscis 0.27% (1/373 anomalies), in case MDB434
Craniofacial dysmorphism 0.27% (1/373 anomalies), in case MDB434
Bulbous nose 0.27% (1/373 anomalies), in case MDB443
Absence of the Septum Pellucidum 0.27% (1/373 anomalies), in case MDB443
Renal agenesis, bilateral 0.27% (1/373 anomalies), in case MDB455
Ureter agenesis, bilateral 0.27% (1/373 anomalies), in case MDB455
Prominent and pointed nose 0.27% (1/373 anomalies), in case MDB470
Anencephaly 0.27% (1/373 anomalies), in case MDB496
Anencephaly facies 0.27% (1/373 anomalies), in case MDB496
Camptodactyly, unilateral 0.27% (1/373 anomalies), in case MDB496
Hypoplasia of diaphragm 0.27% (1/373 anomalies), in case MDB506
Brachydactyly 0.27% (1/373 anomalies), in case MDB514
Hand edema 0.27% (1/373 anomalies), in case MDB514
Narrow thorax 0.27% (1/373 anomalies), in case MDB514
Splenic hypoplasia 0.27% (1/373 anomalies), in case MDB514
Partial agenesis of the corpus callosum (PACC) 0.27% (1/373 anomalies), in case MDB520
Rocker-bottom feet 0.27% (1/373 anomalies), in case MDB532
Persistent truncus arteriosus 0.27% (1/373 anomalies), in case MDB532
Crossed fused renal ectopia 0.27% (1/373 anomalies), in case MDB532
Triploidy, Maternal, nonmolar (triploidy by digyny) 0.27% (1/373 anomalies), in case MDB543
Large nose, fetal 0.27% (1/373 anomalies), in case MDB543
Macrostomia 0.27% (1/373 anomalies), in case MDB543
shoulder edema, fetal 0.27% (1/373 anomalies), in case MDB203
Multicystic renal dysplasia, unilateral 0.27% (1/373 anomalies), in case MDB203
Renal hypoplasia, bilateral 0.27% (1/373 anomalies), in case MDB203
Amnion nodosum 0.27% (1/373 anomalies), in case MDB203
Oligohydramnios 0.27% (1/373 anomalies), in case MDB203
Bowing of long bones 0.27% (1/373 anomalies), in case MDB292
Osteogenesis imperfecta, Type II 0.27% (1/373 anomalies), in case MDB292
Decreased skull bone mineralization 0.27% (1/373 anomalies), in case MDB292
Holoprosencephaly, lobar 0.27% (1/373 anomalies), in case MDB263
Single cerebral ventricule 0.27% (1/373 anomalies), in case MDB263
Thalamic nuclei centrum medianum fusion 0.27% (1/373 anomalies), in case MDB263
Absence of first finger, unilateral 0.27% (1/373 anomalies), in case MDB263
Fissure of the upper gingiva, fetal 0.27% (1/373 anomalies), in case MDB263
Lobulated, fused and horseshoe kidney 0.27% (1/373 anomalies), in case MDB310
Long umbilical cord 0.27% (1/373 anomalies), in case MDB310
Hypoplasia and dysplasia of the kidney, bilateral 0.27% (1/373 anomalies), in case MDB324
Megacystis 0.27% (1/373 anomalies), in case MDB324
Dilatation of ureter , bilateral, congenital 0.27% (1/373 anomalies), in case MDB324
Potter deformity sequence 0.27% (1/373 anomalies), in case MDB324
Potter's facies 0.27% (1/373 anomalies), in case MDB324
Pericardial effusion 0.27% (1/373 anomalies), in case MDB324
Pleural effusion, fetal 0.27% (1/373 anomalies), in case MDB324

Terminology and coding

References

No reference related to Neck edema is available at the moment.

Last modified: 2008-12-22 14:15:59 by farideh

Created: 2008-08-19 19:27:16 by farideh

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