Caffey disease

Infantile cortical hyperostosis is a self-limited inflammatory disorder of infants that causes bone changes, soft tissue swelling and irritability. The disease may be present at birth or occur shortly thereafter. [Source: Wikipedia ]

Synonyms
Caffey disease including infantile and attenuated forms
Caffey-Silverman syndrome
Caffey-Smyth disease
De Toni-Caffey disease
Infantile cortical hyperostosis
Röske-de Toni-Caffey-Smyth disease
OrphaNet reference
Caffey disease 
Subtypes
Caffey disease severe variants with prenatal onset
May Cause
Acquired skull defect
Bowed bones
Broad tubular bones
Clavicular lesion in an infant or child
Congenital widespread osteosclerosis
Cortical bone thickening
Exophthalmos
Humerus-radius-ulna synostosis
Hyperphosphatasemia
Increased soft-tissue interstitial markings
Limb asymmetry
Localized bone overgrowth
Localized cortical bone thickening
Localized periosteal reaction
Mandibular periostitis
Micrognathia
Multiple expanding rib lesions
Multiple opaque jaw lesions
Multiple osteosclerotic bone lesions
Multiple radiolucent bone lesions
Orbital wall sclerosis
Osteosclerosis
Periosteal cloaking
Periosteal new bone formation in a child
Periosteal reaction involving the clavicle
Polyostotic bone lesions in an infant or young child
Radiolucent skull lesion
Radioulnar synostosis
Rib lesion in a child
Scapular lesion in an infant or child
Sclerosis of bone with periosteal reaction
Sclerosis of the orbital roof
Sclerotic clavicle
Severe inflammatory periostitis
Spiculated periosteal reaction
Synostosis of tubular bones
Thick clavicle
Thick periosteal reaction along bone shaft
Thick ribs
Thrombocytosis
Tubular bone synostosis
Unilateral exophthalmos
Wide diametaphysis
Widespread cortical bone thickening
Widespread osteosclerosis
Widespread periosteal reaction
Widespread predominantly cortical osteosclerosis
Caffey disease including infantile and attenuated forms
Caffey-Silverman syndrome
Caffey-Smyth disease
De Toni-Caffey disease
Infantile cortical hyperostosis
Röske-de Toni-Caffey-Smyth disease