Van den Ende-Gupta syndrome- MedGen UID:
- 322127
- •Concept ID:
- C1833136
- •
- Disease or Syndrome
Van den Ende-Gupta syndrome (VDEGS) is an autosomal recessive disorder characterized by severe contractual arachnodactyly from birth and distinctive facial dysmorphism, including triangular face, malar hypoplasia, narrow nose, everted lips, and blepharophimosis. Skeletal anomalies include slender ribs, hooked clavicles, and dislocated radial head. There is no neurologic involvement (summary by Patel et al., 2014).
Van Bogaert-Hozay syndrome- MedGen UID:
- 341263
- •Concept ID:
- C1848598
- •
- Disease or Syndrome
Upper limb mesomelic dysplasia- MedGen UID:
- 1811806
- •Concept ID:
- C5574958
- •
- Disease or Syndrome
This syndrome is an isolated upper limb mesomelic dysplasia. It has been described in four patients from two unrelated families (a man and his daughter, and a Lebanese man and his son). Patients present with ulnar hypoplasia with severe radial bowing, but normal stature. The mode of transmission is likely to be autosomal dominant with variable expressivity.