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Epicanthus

DA: 317

Developmental anomaly information

Definition: An epicanthal fold is skin of the upper eyelid, from the nose to the inner side of the eyebrow, that covers the inner corner (canthus) of the eye.

Synonyms:

Epicanthal fold
Plica palpebronasalis

Developmental anomaly parent: Facial dysmorphism	Topology: Human body > Head and neck > Head > Face > Eyes
System: Human body > Nervous system > Sensory organs > Eyes	Developmental anomaly category: Malformation

Case records MDB5, MDB23, MDB24, MDB29, MDB32, MDB124, MDB125, MDB132, MDB134, MDB135, MDB139, MDB151, MDB178, MDB197, MDB200, MDB214, MDB217, MDB341, MDB36

Links

Observed in MDB cases

In malformative diseases :

del(10)(p12p14) disease

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 :

Facial dysmorphism 8.7% (14/161 anomalies), in cases MDB5, MDB24, MDB29, MDB32, MDB124, MDB125, MDB134, MDB139, MDB151, MDB178, MDB200, MDB214, MDB217, MDB36
Hypertelorism 5.59% (9/161 anomalies), in cases MDB124, MDB125, MDB135, MDB139, MDB151, MDB178, MDB197, MDB214, MDB217
Pulmonary hypoplasia 4.35% (7/161 anomalies), in cases MDB23, MDB29, MDB125, MDB135, MDB200, MDB214, MDB36
Transverse palmar crease, bilateral 3.73% (6/161 anomalies), in cases MDB5, MDB32, MDB124, MDB125, MDB132, MDB134
Low-set ears 3.73% (6/161 anomalies), in cases MDB29, MDB124, MDB134, MDB151, MDB214, MDB217
Macroglossia 3.11% (5/161 anomalies), in cases MDB5, MDB24, MDB32, MDB200, MDB341
Dilatation of ureter , bilateral, congenital 2.48% (4/161 anomalies), in cases MDB5, MDB23, MDB125, MDB341
Clindodactyly of 5th finger, bilateral 2.48% (4/161 anomalies), in cases MDB23, MDB132, MDB200, MDB217
Nonimmune hydrops fetalis (NIHF) 2.48% (4/161 anomalies), in cases MDB125, MDB135, MDB214, MDB36
Talipes equinovarus, bilateral 1.86% (3/161 anomalies), in cases MDB5, MDB29, MDB341
Single transverse palmar crease, unilateral 1.86% (3/161 anomalies), in cases MDB24, MDB197, MDB341
Mongoloid slope of the palpebral fissures 1.86% (3/161 anomalies), in cases MDB24, MDB197, MDB200
Placenta hypoplasia 1.86% (3/161 anomalies), in cases MDB29, MDB139, MDB200
Broad nasal bridge 1.86% (3/161 anomalies), in cases MDB124, MDB132, MDB135
Coarctation of aorta, 1.86% (3/161 anomalies), in cases MDB125, MDB135, MDB178
Micrognathia 1.86% (3/161 anomalies), in cases MDB134, MDB200, MDB217
Pleural effusion, fetal 1.86% (3/161 anomalies), in cases MDB135, MDB197, MDB214
Flat face 1.24% (2/161 anomalies), in cases MDB5, MDB36
Intestinal malrotation 1.24% (2/161 anomalies), in cases MDB5, MDB125
Cystic hygroma 1.24% (2/161 anomalies), in cases MDB5, MDB135
Multicystic renal dysplasia,bilateral 1.24% (2/161 anomalies), in cases MDB23, MDB29
Sloping forehead 1.24% (2/161 anomalies), in cases MDB24, MDB200
Neck edema 1.24% (2/161 anomalies), in cases MDB29, MDB200
Foot edema 1.24% (2/161 anomalies), in cases MDB29, MDB132
Macrocephaly 1.24% (2/161 anomalies), in cases MDB125, MDB217
Hand edema 1.24% (2/161 anomalies), in cases MDB132, MDB135
Ascites, fetal 1.24% (2/161 anomalies), in cases MDB135, MDB214
Flattened occiput 0.62% (1/161 anomalies), in case MDB5
Atrial Hypertrophy 0.62% (1/161 anomalies), in case MDB5
Overlapping toes 0.62% (1/161 anomalies), in case MDB5
Preauricular hamartoma 0.62% (1/161 anomalies), in case MDB5
Ventricular septal defect, membranous 0.62% (1/161 anomalies), in case MDB5
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.62% (1/161 anomalies), in case MDB5
Fusion of the adrenal glands 0.62% (1/161 anomalies), in case MDB5
Microsplenia 0.62% (1/161 anomalies), in case MDB5
Lung agenesis, unilateral 0.62% (1/161 anomalies), in case MDB5
Unilobate lung, unilateral 0.62% (1/161 anomalies), in case MDB5
Bladder wall thickness 0.62% (1/161 anomalies), in case MDB5
Amnion nodosum 0.62% (1/161 anomalies), in case MDB5
Polysplenia 0.62% (1/161 anomalies), in case MDB5
Hydronephrosis, congenital, bilateral 0.62% (1/161 anomalies), in case MDB23
Renal pelvis dilatation, bilateral 0.62% (1/161 anomalies), in case MDB23
Synophrys 0.62% (1/161 anomalies), in case MDB24
Giant omphalocele 0.62% (1/161 anomalies), in case MDB29
Long philtrum 0.62% (1/161 anomalies), in case MDB29
Axillary pterygia,unilateral 0.62% (1/161 anomalies), in case MDB29
Tridactyly, unilateral 0.62% (1/161 anomalies), in case MDB29
vertebral bones and gracile ribs with multiple abnormalities 0.62% (1/161 anomalies), in case MDB29
Small round skull 0.62% (1/161 anomalies), in case MDB32
Wide space between 1st and 2nd toes, unilateral 0.62% (1/161 anomalies), in case MDB124
Atrioventricular - channel 0.62% (1/161 anomalies), in case MDB125
Hypoplasia of the aortic isthmus 0.62% (1/161 anomalies), in case MDB125
Defective developement of left ventricle 0.62% (1/161 anomalies), in case MDB125
Retroplacental hemorrhage 0.62% (1/161 anomalies), in case MDB134
Infarcted placenta 0.62% (1/161 anomalies), in case MDB134
Dolicocephaly 0.62% (1/161 anomalies), in case MDB134
Periventricular Leukomalacia (PVL) 0.62% (1/161 anomalies), in case MDB134
Pulmonary artery dilatation, fetal 0.62% (1/161 anomalies), in case MDB135
Lobulated, fused and horseshoe kidney 0.62% (1/161 anomalies), in case MDB135
Intrauterine growth retardation, symmetric 0.62% (1/161 anomalies), in case MDB135
Transverse aortic hypoplasia 0.62% (1/161 anomalies), in case MDB135
Corpus callosum agenesis 0.62% (1/161 anomalies), in case MDB139
Clindodactyly of 5th finger, unilateral 0.62% (1/161 anomalies), in case MDB139
Neuroepithelial cysts of the third ventricule,congenital 0.62% (1/161 anomalies), in case MDB139
Relative Macrocephaly 0.62% (1/161 anomalies), in case MDB151
Dysplasia of deep nuclei (olive dysplasia) 0.62% (1/161 anomalies), in case MDB151
Left ventricular hypertrophy, 0.62% (1/161 anomalies), in case MDB178
long straight nose 0.62% (1/161 anomalies), in case MDB178
Retrognathia 0.62% (1/161 anomalies), in case MDB178
cutaneous edema, fetal 0.62% (1/161 anomalies), in case MDB197
Nasal hypoplasia 0.62% (1/161 anomalies), in case MDB200
Recessed forehead 0.62% (1/161 anomalies), in case MDB200
Flattened nose 0.62% (1/161 anomalies), in case MDB214
Badly-hemmed ears 0.62% (1/161 anomalies), in case MDB214
Cerebral ventriculomegaly 0.62% (1/161 anomalies), in case MDB217
Hydrocephalus 0.62% (1/161 anomalies), in case MDB217
Prominent and pointed nose 0.62% (1/161 anomalies), in case MDB217
Prominence of nasofrontal angle 0.62% (1/161 anomalies), in case MDB217
Short neck 0.62% (1/161 anomalies), in case MDB341
Microstomia 0.62% (1/161 anomalies), in case MDB341
Subcapsular renal cyst, 0.62% (1/161 anomalies), in case MDB341
Thin upper lip 0.62% (1/161 anomalies), in case MDB36
Relative Microcephaly 0.62% (1/161 anomalies), in case MDB36
Ventricular septal defect, muscular 0.62% (1/161 anomalies), in case MDB36
Renal hypoplasia 0.62% (1/161 anomalies), in case MDB36

Terminology and coding

References

No reference related to Epicanthus is available at the moment.

Last modified: 2008-12-16 17:43:18 by farideh

Created: 2008-06-02 02:00:00 by phsaw

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