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Case Reports |

INFANTILE CORTICAL HYPEROSTOSIS

VINCENT DE PAUL LARKIN, M.D.; PAUL ROUSSEAU, M.D.
Am J Dis Child. 1950;79(1):105-110. doi:10.1001/archpedi.1950.04040010115013.
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SEVERAL cases of the syndrome of infantile cortical hyperostosis have been reported since Caffey and Silverman1 first described this heretofore unknown disease of infants. Smyth, Potter and Silverman2 were among the early workers to add to the rapidly growing number of cases. These were followed with reports by Whipple,3 Dickson and his associates,4 Shuman5 and Gipson and Clark6 and from the Children's Hospital, Washington, D. C.7 The purpose of this report is to present 2 additional cases of this syndrome and to discuss some variable aspects of the disease.

REPORT OF CASES  Case 1.—M. A. F., a 5 month old Italian infant, was admitted to the babies' wards of the New York Post-Graduate Hospital on Nov. 11, 1947 because of a facial swelling since 2 weeks of age.Family History.—The parents were living and in good health. There were no known familial

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Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

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