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Gnathodiaphyseal dysplasia
rareGnathodiaphyseal 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.
- Identifiers
- MONDO:0008151 OMIM:166260Orphanet:53697
- Causal genes
- ANO5
- Also known as
- GDD · Levin syndrome 2 · osteogenesis imperfecta Levin type
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