radial ray defects
Image Gallery
[ (||image_reduire{0,60}|inserer_attribut{alt,Radial agenesis with ectrodactyly}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,Radial agenesis with ectrodactyly}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,First metacarpal severe hypoplasia}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,First metacarpal severe hypoplasia}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,Omphalocele-radial ray aplasia association}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,Omphalocele-radial ray aplasia association}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,Omphalocele-radial ray aplasia association}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ] [ (||image_reduire{0,60}|inserer_attribut{alt,}) ]
Types
radial agenesis (radial aplasia)
radial hypoplasia
preaxial polydactyly
anomalies of thumbs
- triphalangeal thumbs
- supernumerary thumbs
- broad thumb
- bifid thumb
Associations
omphalocele (#2359107#)
diaphragmatic hernia (#2359107#)
hepatic cyst (#2359107#)
Types
isolated radial agenesis
X-linked radial agenesis (X-linked radial ray deficiency) (MIM.300378)
Syndromal types
VATER association (VACTERL association)
Fanconi disease (Fanconi syndrome or Fanconi anemia)
Pallister-Hall syndrome
Cateye syndrome
Duane anomaly with thenar hypoplasia (Duane-radial ray syndrome or Okihiro syndrome) (MIM.607323) (SALL4 mutations)
craniosynostosis with radial defects
- Baller-Gerold syndrome (MIM.218600)
- Saethre-Chotzen syndrome (SCS) (MIM.101400)
hemifacial microsomia with radial defects (Goldenhar syndrome with radial defects) (MIM.141400)
IVIC syndrome (oculootoradial syndrome) (MIM.147750)
congenital posterior dislocation of radial heads (MIM.179200)
radial apladia with cleft lip/palate (MIM.179400)
X-linked dominant syndrome of radioulnar synostosis and radial ray abnormalities with severe malformations in the male and milder features in females (MIM.300233)
radialrenal syndrome (MIM.179280)
radial ray defects, omphalocele, diaphragmatic hernia, and hepatic cyst association (Gershoni-Baruch syndrome) (MIM.609545) (HP.9455)
omphalocele-radial ray aplasia association (ORR) (HP.12202)
Case records
Case 10516: Sirenomelia with bilateral radial ray anomalies
See also
limb malformations (limb anomalies)