Gnathodiaphyseal dysplasia

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.

Also known as: GDD, gnathodiaphyseal dysplasia, GNATHODIAPHYSEAL dysplasia, Gnathodiaphyseal sclerosis, Levin syndrome 2, osteogenesis imperfecta Levin type, osteogenesis imperfecta with unusual skeletal lesions

35 clinical trials for this condition and its sub-types.