Caffey Syndrome (Caffey-Silverman Syndrome; Infantile Cortical Hyperostosis)& 848g68i nbsp; & 848g68i nbsp; & 848g68i nbsp; & 848g68i nbsp; & 848g68i nbsp; & 848g68i nbsp; 185
General: Cause unknown, possibly collagen disease or viral infection; prevalent in females; onset in early infancy; sudden onset; benign; self-limited.
Ocular: Periorbital edema and tenderness; transient proptosis; mild conjunctivitis.
Clinical: Tender swelling over regions of cortical hyperostosis (may resemble periostitis); severe anemia; fever; dysphagia; pleurisy.
Borochowitz Z, et al. Familial Caffey's disease and late recurrence in a child. Clin Genet 1991; 40:329-335.
Caffey J, Silvermann WA. Infantile cortical hyperostoses. Preliminary report of a new syndrome. Am J Roentgenol 1945; 54:1.
Keeton BR. Vitamin E deficiency and thrombocytosis in Caffey's disease. Arch Dis Child 1976; 51:393-395.
Minton LR, Elliott JR. Ocular manifestations of infantile cortical hyperostosis. Am J Ophthalmol 1967; 64:902.
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