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Transverse palmar crease, bilateral

DA: 198

Developmental anomaly information

Definition: In humans, a single transverse palmar crease is a single crease that extends across the palm of the hand, formed by the fusion of the two palmar creases that people typically have. The presence of a single transverse palmar crease can be, but is not always, a symptom of certain medical conditions such as Fetal alcohol syndrome and genetic abnormalities including Down syndrome and Noonan syndrome. Males are twice as likely as females to have this condition.

Synonyms:

simian crease
simian line

Developmental anomaly parent: (empty)	Topology: Human body > Limbs > Upper limbs > Hand
System: integument & skin	Developmental anomaly category: Malformation

Case records MDB5, MDB30, MDB32, MDB99, MDB121, MDB124, MDB125, MDB132, MDB134, MDB142, MDB199, MDB227, MDB362, MDB363, MDB368, MDB432, MDB440, MDB441, MDB443, MDB448, MDB481, MDB515, MDB535, MDB4, MDB146, MDB265

Links

Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (MDB)

() in cases MDB, MDB, MDB, 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 6.19% (13/210 anomalies), in cases MDB5, MDB30, MDB32, MDB124, MDB125, MDB134, MDB142, MDB227, MDB440, MDB443, MDB448, MDB481, MDB515
Hypertelorism 3.81% (8/210 anomalies), in cases MDB124, MDB125, MDB227, MDB363, MDB368, MDB448, MDB481, MDB515
Low-set ears 3.81% (8/210 anomalies), in cases MDB124, MDB134, MDB227, MDB362, MDB441, MDB443, MDB515, MDB146
Clindodactyly of 5th finger, bilateral 3.81% (8/210 anomalies), in cases MDB132, MDB142, MDB362, MDB368, MDB481, MDB515, MDB535, MDB4
Macroglossia 3.33% (7/210 anomalies), in cases MDB5, MDB30, MDB32, MDB121, MDB227, MDB432, MDB4
Epicanthus 2.86% (6/210 anomalies), in cases MDB5, MDB32, MDB124, MDB125, MDB132, MDB134
Intrauterine growth retardation, symmetric 2.38% (5/210 anomalies), in cases MDB99, MDB199, MDB368, MDB481, MDB265
Toe hypoplasia, first, bilateral 2.38% (5/210 anomalies), in cases MDB362, MDB368, MDB441, MDB448, MDB146
Short neck 2.38% (5/210 anomalies), in cases MDB363, MDB368, MDB432, MDB440, MDB441
Low nasal bridge 2.38% (5/210 anomalies), in cases MDB368, MDB432, MDB443, MDB515, MDB146
Pulmonary hypoplasia 1.9% (4/210 anomalies), in cases MDB30, MDB125, MDB227, MDB443
Neck edema 1.9% (4/210 anomalies), in cases MDB121, MDB227, MDB368, MDB443
Retrognathia 1.9% (4/210 anomalies), in cases MDB368, MDB481, MDB146, MDB265
Dilatation of ureter , bilateral, congenital 1.43% (3/210 anomalies), in cases MDB5, MDB125, MDB432
Talipes equinovarus, bilateral 1.43% (3/210 anomalies), in cases MDB5, MDB362, MDB363
Single umblical artery (SUA)-Isolated 1.43% (3/210 anomalies), in cases MDB30, MDB99, MDB448
Micrognathia 1.43% (3/210 anomalies), in cases MDB134, MDB363, MDB448
Ventricular septal defect, muscular 1.43% (3/210 anomalies), in cases MDB440, MDB515, MDB4
Rocker-bottom feet 1.43% (3/210 anomalies), in cases MDB440, MDB481, MDB515
Corpus callosum agenesis 1.43% (3/210 anomalies), in cases MDB441, MDB443, MDB481
Absence of the Septum Pellucidum 1.43% (3/210 anomalies), in cases MDB441, MDB443, MDB481
Flat face 0.95% (2/210 anomalies), in cases MDB5, MDB227
Flattened occiput 0.95% (2/210 anomalies), in cases MDB5, MDB227
Overlapping toes 0.95% (2/210 anomalies), in cases MDB5, MDB448
Intestinal malrotation 0.95% (2/210 anomalies), in cases MDB5, MDB125
Wide space between 1st and 2nd toes, unilateral 0.95% (2/210 anomalies), in cases MDB30, MDB124
Aberrant right subclavian artery 0.95% (2/210 anomalies), in cases MDB30, MDB440
Atrioventricular - channel 0.95% (2/210 anomalies), in cases MDB121, MDB125
Broad nasal bridge 0.95% (2/210 anomalies), in cases MDB124, MDB132
Coarctation of aorta, 0.95% (2/210 anomalies), in cases MDB125, MDB142
Nonimmune hydrops fetalis (NIHF) 0.95% (2/210 anomalies), in cases MDB125, MDB481
Retroplacental hemorrhage 0.95% (2/210 anomalies), in cases MDB134, MDB368
Dolicocephaly 0.95% (2/210 anomalies), in cases MDB134, MDB481
Cerebral ventriculomegaly 0.95% (2/210 anomalies), in cases MDB199, MDB481
Mongoloid slope of the palpebral fissures 0.95% (2/210 anomalies), in cases MDB227, MDB515
Brachydactyly 0.95% (2/210 anomalies), in cases MDB362, MDB441
Posteriorly inclined and low-positioned ears 0.95% (2/210 anomalies), in cases MDB440, MDB481
Lobulated, fused and horseshoe kidney 0.95% (2/210 anomalies), in cases MDB440, MDB265
Thymic hypoplasia 0.95% (2/210 anomalies), in cases MDB440, MDB481
Pulmonary artery hypoplasia 0.95% (2/210 anomalies), in cases MDB481, MDB535
Dextroposition of aorta 0.95% (2/210 anomalies), in cases MDB481, MDB535
Ureteral duplication, complete, unilateral 0.95% (2/210 anomalies), in cases MDB481, MDB146
Atrial Hypertrophy 0.48% (1/210 anomalies), in case MDB5
Preauricular hamartoma 0.48% (1/210 anomalies), in case MDB5
Ventricular septal defect, membranous 0.48% (1/210 anomalies), in case MDB5
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.48% (1/210 anomalies), in case MDB5
Fusion of the adrenal glands 0.48% (1/210 anomalies), in case MDB5
Microsplenia 0.48% (1/210 anomalies), in case MDB5
Cystic hygroma 0.48% (1/210 anomalies), in case MDB5
Lung agenesis, unilateral 0.48% (1/210 anomalies), in case MDB5
Unilobate lung, unilateral 0.48% (1/210 anomalies), in case MDB5
Bladder wall thickness 0.48% (1/210 anomalies), in case MDB5
Amnion nodosum 0.48% (1/210 anomalies), in case MDB5
Polysplenia 0.48% (1/210 anomalies), in case MDB5
Pleural effusion, fetal 0.48% (1/210 anomalies), in case MDB30
Small round skull 0.48% (1/210 anomalies), in case MDB32
Patent Foramen Ovale 0.48% (1/210 anomalies), in case MDB121
Mitral valve stenosis 0.48% (1/210 anomalies), in case MDB121
Duodenal atresia and stenosis, congenital 0.48% (1/210 anomalies), in case MDB121
Hypoplasia of the aortic isthmus 0.48% (1/210 anomalies), in case MDB125
Defective developement of left ventricle 0.48% (1/210 anomalies), in case MDB125
Macrocephaly 0.48% (1/210 anomalies), in case MDB125
Hand edema 0.48% (1/210 anomalies), in case MDB132
Foot edema 0.48% (1/210 anomalies), in case MDB132
Infarcted placenta 0.48% (1/210 anomalies), in case MDB134
Periventricular Leukomalacia (PVL) 0.48% (1/210 anomalies), in case MDB134
Wide space between 1st and 2nd toes, bilateral 0.48% (1/210 anomalies), in case MDB142
Placenta hypoplasia 0.48% (1/210 anomalies), in case MDB199
Absence of one paire the rib 0.48% (1/210 anomalies), in case MDB227
Hydronephrosis, congenital, bilateral 0.48% (1/210 anomalies), in case MDB432
Brachydactyly of the toes 0.48% (1/210 anomalies), in case MDB432
Flattened nose 0.48% (1/210 anomalies), in case MDB440
Short philtrum 0.48% (1/210 anomalies), in case MDB440
Gastroschisis 0.48% (1/210 anomalies), in case MDB440
Polydactyly,of the hand, postaxial 0.48% (1/210 anomalies), in case MDB440
Flexion contracture of the fingers 0.48% (1/210 anomalies), in case MDB440
dextro-Transposition of the great arteries 0.48% (1/210 anomalies), in case MDB440
Adrenal hypoplasia, fetal 0.48% (1/210 anomalies), in case MDB440
Bulbous nose 0.48% (1/210 anomalies), in case MDB443
Hypogenesis of the Cerebellar Vermis 0.48% (1/210 anomalies), in case MDB443
Communicating hydrocephalus 0.48% (1/210 anomalies), in case MDB443
Acrocephaly 0.48% (1/210 anomalies), in case MDB448
Large nose, fetal 0.48% (1/210 anomalies), in case MDB448
Placenta villous fibrosis 0.48% (1/210 anomalies), in case MDB448
Ambiguous genitalia 0.48% (1/210 anomalies), in case MDB481
Cleft palate, bilateral 0.48% (1/210 anomalies), in case MDB481
Imperforate Anus 0.48% (1/210 anomalies), in case MDB481
Persistent left superior vena cava 0.48% (1/210 anomalies), in case MDB481
Renal hypoplasia, unilateral 0.48% (1/210 anomalies), in case MDB481
Renal agenesis, unilateral 0.48% (1/210 anomalies), in case MDB481
Presence of an infantile uterus with both testes 0.48% (1/210 anomalies), in case MDB481
Probst bundle 0.48% (1/210 anomalies), in case MDB481
Tetralogy of Fallot 0.48% (1/210 anomalies), in case MDB535
Right ventricular hypertrophy 0.48% (1/210 anomalies), in case MDB535
Hypoplasia of the humerus, bilateral 0.48% (1/210 anomalies), in case MDB4
Autosomal Recessive Polycystic Kidney Disease 0.48% (1/210 anomalies), in case MDB146
Nephromegaly, bilateral 0.48% (1/210 anomalies), in case MDB146
Renal-hepatic-pancreatic dysplasia 0.48% (1/210 anomalies), in case MDB146
Renal pelvis dilatation, unilateral 0.48% (1/210 anomalies), in case MDB146
Clindodactyly of 5th finger, unilateral 0.48% (1/210 anomalies), in case MDB146
Potter's facies 0.48% (1/210 anomalies), in case MDB146
Thumb agenesis, bilateral 0.48% (1/210 anomalies), in case MDB265
absence of radius, bilateral 0.48% (1/210 anomalies), in case MDB265
Ulna,absence of, bilateral 0.48% (1/210 anomalies), in case MDB265

Terminology and coding

References

No reference related to Transverse palmar crease, bilateral is available at the moment.

Last modified: 2008-12-16 16:47:30 by farideh

Created: 2008-05-13 00:00:00 by phsaw

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