Infantile cortical hyperostosis

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Infantile cortical hyperostosis
File:Infantile cortical hyperostosis.jpg
Synonyms Caffey disease, Caffey-Silverman syndrome
Pronounce N/A
Specialty N/A
Symptoms Fever, irritability, swelling of soft tissues, bone changes
Complications Deformity of bones, pain
Onset Typically in infancy
Duration Self-limiting, usually resolves by age 2
Types N/A
Causes Unknown, possibly genetic
Risks Family history of the condition
Diagnosis Clinical diagnosis, X-ray
Differential diagnosis Osteomyelitis, child abuse, scurvy
Prevention N/A
Treatment Supportive care, analgesics
Medication Nonsteroidal anti-inflammatory drugs (NSAIDs)
Prognosis Generally good, resolves with time
Frequency Rare
Deaths N/A


Infantile cortical hyperostosis is a rare, 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. The cause is unknown.

Symptoms[edit]

The symptoms of infantile cortical hyperostosis may include the following:

Causes[edit]

The exact cause of infantile cortical hyperostosis is unknown. Some researchers believe it may be related to a viral infection. Others believe it may be a genetic disorder.

Diagnosis[edit]

The diagnosis of infantile cortical hyperostosis is usually made based on the clinical symptoms and physical examination. Imaging studies such as X-rays or CT scans may be used to confirm the diagnosis.

Treatment[edit]

Treatment for infantile cortical hyperostosis is usually supportive, as the condition often resolves on its own. This may include pain management and physical therapy to maintain joint mobility and prevent contractures.

Prognosis[edit]

The prognosis for infantile cortical hyperostosis is generally good. Most children with the condition recover completely with no lasting effects. However, in severe cases, there may be permanent deformity or functional impairment.

See also[edit]

References[edit]