osteogenesis imperfecta type IV - moderately severe disease
Last reviewed 01/2018
Type IV osteogenesis imperfecta a moderately severe form of the condition.
Type IV is differentiated from the type I form by white sclera, and from the type III form by not being progressively deforming.
- with respect
to classification of osteogenesis imperfecta
- the broad clinical and biomolecular spectrum mean that any classification is unable to be complete or accurate - however it represents a practical tool for the clinician dealing with management of patients