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Familial Caffey's disease (medical condition): A rare inflammatory disorder that affects bones and soft tissue in infants. The condition may affect virtually any bone and causes excessive enlargement of part of the bone (cortex). Infant feeding problems may occur if the jaw bone is affected which can affect weight gain. The inflammatory course of the disease eventually stops and over time the bones remodel to a normal appearance.
See also:
Hyperostosis cortical infantile:
»Introduction: Hyperostosis cortical infantile
»Symptoms of Hyperostosis cortical infantile
These medical condition or symptom topics may be relevant to medical information for Familial Caffey's disease:
Familial Caffey's disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Familial Caffey's disease, or a subtype of Familial Caffey's disease,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Familial Caffey's disease: Another name for Hyperostosis cortical infantile (or close medical condition association).
»Introduction: Hyperostosis cortical infantile
»Symptoms of Hyperostosis cortical infantile
Some of the symptoms of Familial Caffey's disease incude:
See full list of 6 symptoms of Familial Caffey's disease (Hyperostosis cortical infantile)
Source - NIH
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