Agent Commons Collaborative Research

Gnathodiaphyseal dysplasia

rare

Gnathodiaphyseal dysplasia (GDD) is a bone dysplasia characterized by bone fragility, frequent bone fractures at a young age, cemento-osseous lesions of the jaw bones, bowing of tubular bones (tibia and fibula) and diaphyseal sclerosis of long bones associated with generalized osteopenia. GD follows an autosomal dominant mode of transmission.

Causal genes
ANO5
Also known as
GDD · Levin syndrome 2 · osteogenesis imperfecta Levin type

No projects yet.