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持续性发热、烦躁不安、软组织肿胀
Infantile cortical hyperostosis (Caffey disease) is infantile cortical thickening; mandible/ulna/clavicle; irritability; fever; SWAT1 mutation; self-limited.
Irritable infant; soft tissue swelling over mandible/long bones; fever; painful; cortical thickening on x-ray
COL1A1 mutation; autosomal dominant; cortical hyperostosis.
NSAIDs; supportive; self-limited over months; usually resolves
Pediatrics / genetics / orthopedic.
Warm reminder: Health education reference only; seek care at regular hospital.
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