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Polydactyly,of the hand, postaxial

DA: 8

Developmental anomaly information

Definition: Postaxial hand polydactyly is a common isolated disorder in African black and African American children, and autosomal dominant transmission is suspected. Postaxial polydactyly is approximately 10 times more frequent in blacks than in whites and is more frequent in male children. In contrast, postaxial polydactyly seen in white children is usually syndromic and associated with an autosomal recessive transmission.

Developmental anomaly parent: (empty)	Topology: Human body > Limbs > Upper limbs > Hand
System: Human body > musculoskeletal system.	Developmental anomaly category: Malformation

Case records MDB155, MDB340, MDB346, MDB440, MDB463, MDB473, MDB501, MDB509, MDB510, MDB18, MDB301

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Observed in MDB cases

Observed in combinaisons (MDB)

Observed in malformative diseases (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 3.6% (5/139 anomalies), in cases MDB340, MDB346, MDB440, MDB463, MDB473
Pulmonary hypoplasia 2.88% (4/139 anomalies), in cases MDB155, MDB463, MDB509, MDB510
Aberrant right subclavian artery 2.16% (3/139 anomalies), in cases MDB155, MDB440, MDB463
Holoprosencephaly, alobar 2.16% (3/139 anomalies), in cases MDB340, MDB463, MDB18
Proboscis 2.16% (3/139 anomalies), in cases MDB340, MDB463, MDB18
Intrauterine growth retardation, symmetric 2.16% (3/139 anomalies), in cases MDB340, MDB473, MDB18
Placenta hypoplasia 2.16% (3/139 anomalies), in cases MDB463, MDB473, MDB301
Single umblical artery (SUA)-Isolated 1.44% (2/139 anomalies), in cases MDB155, MDB501
Cyclopia 1.44% (2/139 anomalies), in cases MDB340, MDB18
Hypoplasia of ascending aorta 1.44% (2/139 anomalies), in cases MDB340, MDB301
Defective developement of left ventricle 1.44% (2/139 anomalies), in cases MDB340, MDB463
Bicornuate uterus 1.44% (2/139 anomalies), in cases MDB340, MDB301
Single cerebral ventricule 1.44% (2/139 anomalies), in cases MDB340, MDB473
Thalamic nuclei centrum medianum fusion 1.44% (2/139 anomalies), in cases MDB340, MDB18
Hypertelorism 1.44% (2/139 anomalies), in cases MDB346, MDB473
Short philtrum 1.44% (2/139 anomalies), in cases MDB440, MDB473
Posteriorly inclined and low-positioned ears 1.44% (2/139 anomalies), in cases MDB440, MDB501
Microcephaly 1.44% (2/139 anomalies), in cases MDB473, MDB509
Micrognathia 1.44% (2/139 anomalies), in cases MDB473, MDB501
Short rib polydactyly syndrome, type 1 1.44% (2/139 anomalies), in cases MDB509, MDB510
Short femur with angulated shaft 1.44% (2/139 anomalies), in cases MDB509, MDB510
Hypoplasia of optic nerve, bilateral 1.44% (2/139 anomalies), in cases MDB509, MDB510
Narrow thorax 1.44% (2/139 anomalies), in cases MDB509, MDB510
Olfactory bulbs hypoplasia 1.44% (2/139 anomalies), in cases MDB509, MDB510
Abnormal formation of the cerebellar gyri 0.72% (1/139 anomalies), in case MDB155
Gothic palate 0.72% (1/139 anomalies), in case MDB155
Overlapping fingers 0.72% (1/139 anomalies), in case MDB155
Badly-hemmed ears 0.72% (1/139 anomalies), in case MDB155
Omphalocele 0.72% (1/139 anomalies), in case MDB155
Tracheoesophageal fistula (TEF), and esophageal atresia, Type C 0.72% (1/139 anomalies), in case MDB155
Purkinje cell ectopia in the cerebellum 0.72% (1/139 anomalies), in case MDB155
Olfactory nerve, absence of, unilateral 0.72% (1/139 anomalies), in case MDB155
Olfactory nerve hypoplasia,unilateral 0.72% (1/139 anomalies), in case MDB155
Trigonocephaly 0.72% (1/139 anomalies), in case MDB340
Arhinia 0.72% (1/139 anomalies), in case MDB340
Microstomia 0.72% (1/139 anomalies), in case MDB340
Hydronephrosis, congenital, bilateral 0.72% (1/139 anomalies), in case MDB340
Hypoplastic left heart syndrome (HLHS) 0.72% (1/139 anomalies), in case MDB340
Hypoplasia of the aortic isthmus 0.72% (1/139 anomalies), in case MDB340
Mitral valve stenosis 0.72% (1/139 anomalies), in case MDB340
Pulmonary artery dilatation, fetal 0.72% (1/139 anomalies), in case MDB340
Olfactory bulbs, absence of 0.72% (1/139 anomalies), in case MDB340
Olfactory nerve, absence of, bilateral 0.72% (1/139 anomalies), in case MDB340
Optic nerve, absence of, bilateral 0.72% (1/139 anomalies), in case MDB340
Cerebellar hypoplasia 0.72% (1/139 anomalies), in case MDB340
Pachygyria 0.72% (1/139 anomalies), in case MDB340
Dysplastic kidney with tubular cysts 0.72% (1/139 anomalies), in case MDB346
Bladder hypoplasia 0.72% (1/139 anomalies), in case MDB346
Tetralogy of Fallot 0.72% (1/139 anomalies), in case MDB346
Pulmonary valve atresia 0.72% (1/139 anomalies), in case MDB346
Pulmonary artery hypoplasia 0.72% (1/139 anomalies), in case MDB346
Dextroposition of aorta 0.72% (1/139 anomalies), in case MDB346
Right ventricular hypertrophy 0.72% (1/139 anomalies), in case MDB346
Microtia 0.72% (1/139 anomalies), in case MDB346
Malformed ear 0.72% (1/139 anomalies), in case MDB346
Bulbous nose 0.72% (1/139 anomalies), in case MDB346
Renal pelvis dilatation, bilateral 0.72% (1/139 anomalies), in case MDB346
Syndactyly of the toes, complex, bilateral 0.72% (1/139 anomalies), in case MDB346
Talipes equinovarus,unilateral 0.72% (1/139 anomalies), in case MDB346
Meckel diverticulum 0.72% (1/139 anomalies), in case MDB346
Nephromegaly, bilateral 0.72% (1/139 anomalies), in case MDB346
Thin upper lip 0.72% (1/139 anomalies), in case MDB346
Ventricular septal defect, muscular 0.72% (1/139 anomalies), in case MDB440
Flattened nose 0.72% (1/139 anomalies), in case MDB440
Short neck 0.72% (1/139 anomalies), in case MDB440
Gastroschisis 0.72% (1/139 anomalies), in case MDB440
Transverse palmar crease, bilateral 0.72% (1/139 anomalies), in case MDB440
Flexion contracture of the fingers 0.72% (1/139 anomalies), in case MDB440
Rocker-bottom feet 0.72% (1/139 anomalies), in case MDB440
dextro-Transposition of the great arteries 0.72% (1/139 anomalies), in case MDB440
Lobulated, fused and horseshoe kidney 0.72% (1/139 anomalies), in case MDB440
Adrenal hypoplasia, fetal 0.72% (1/139 anomalies), in case MDB440
Thymic hypoplasia 0.72% (1/139 anomalies), in case MDB440
Hypotelorisme 0.72% (1/139 anomalies), in case MDB463
Truncus bicaroticus 0.72% (1/139 anomalies), in case MDB463
Splenomegaly, congenital 0.72% (1/139 anomalies), in case MDB463
Single-nostril nose 0.72% (1/139 anomalies), in case MDB463
Semilobar holoprosencephaly 0.72% (1/139 anomalies), in case MDB473
Corpus callosum agenesis 0.72% (1/139 anomalies), in case MDB473
Deep gray nuclear malformations(the caudate nuclei, thalami,..) 0.72% (1/139 anomalies), in case MDB473
Incomplete cleavage of cerebral hemispheres 0.72% (1/139 anomalies), in case MDB473
Low-set ears 0.72% (1/139 anomalies), in case MDB473
Myelomeningocele,thoracolumbar 0.72% (1/139 anomalies), in case MDB473
Giant omphalocele 0.72% (1/139 anomalies), in case MDB473
Polydactyly of the hand, preaxial 0.72% (1/139 anomalies), in case MDB473
hypoplasia of the rib 0.72% (1/139 anomalies), in case MDB473
Pulmonary valve dysplasia 0.72% (1/139 anomalies), in case MDB473
Tricuspid valve dysplasia 0.72% (1/139 anomalies), in case MDB473
Interauricular communication 0.72% (1/139 anomalies), in case MDB473
Mandibulofacial dysostosis 0.72% (1/139 anomalies), in case MDB501
Polydactyly of the foot 0.72% (1/139 anomalies), in case MDB501
Split-hand/split-foot malformation (SHFM) 0.72% (1/139 anomalies), in case MDB501
Renal agenesis, unilateral 0.72% (1/139 anomalies), in case MDB501
Ureter agenesis, unilateral 0.72% (1/139 anomalies), in case MDB501
Hydroureter, unilateral 0.72% (1/139 anomalies), in case MDB501
Unicorn Uterus 0.72% (1/139 anomalies), in case MDB501
Acro–renal–mandibular syndrome 0.72% (1/139 anomalies), in case MDB501
Micromelia 0.72% (1/139 anomalies), in case MDB509
Hypogenesis of the Cerebellar Vermis 0.72% (1/139 anomalies), in case MDB509
Micromelia, lower limbs 0.72% (1/139 anomalies), in case MDB510
Micropenis 0.72% (1/139 anomalies), in case MDB18
Cortical dysgenesis (CD), diffuse 0.72% (1/139 anomalies), in case MDB18
Cleft palate with cleft lip,bilateral, complete 0.72% (1/139 anomalies), in case MDB301
Aberrant left subclavian artery 0.72% (1/139 anomalies), in case MDB301
Intestinal malrotation 0.72% (1/139 anomalies), in case MDB301

Terminology and coding

References

No reference related to Polydactyly,of the hand, postaxial is available at the moment.

Last modified: 2008-12-17 19:14:52 by farideh

Created: 2008-06-02 11:48:04 by farideh

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