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Arch Dis Child. 1973 October; 48(10): 818–821.
PMCID: PMC1648512

Wiskott-Aldrich syndrome associated with idiopathic infantile cortical hyperostosis (Caffey's disease).

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Selected References

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  • ALDRICH RA, STEINBERG AG, CAMPBELL DC. Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. Pediatrics. 1954 Feb;13(2):133–139. [PubMed]
  • GERRARD JW, HOLMAN GH, GORMAN AA, MORROW IH. Familial infantile cortical hyperostosis. J Pediatr. 1961 Oct;59:543–548. [PubMed]
  • Pickering D, Cuddigan B. Infantile cortical hyperostosis associated with thrombocythaemia. Lancet. 1969 Aug 30;2(7618):464–465. [PubMed]
  • RIVERA AM, BIEHUSEN FC. Aldrich's syndrome. Report of a case with subperiosteal hemorrhage. J Pediatr. 1960 Jul;57:86–88. [PubMed]
  • Stiehm ER, Fudenberg HH. Serum levels of immune globulins in health and disease: a survey. Pediatrics. 1966 May;37(5):715–727. [PubMed]
  • Temperley IJ, Douglas SJ, Rees JP. Raised immunoglobulin levels and thrombocytosis in infantile cortical hyperostosis. Arch Dis Child. 1972 Dec;47(256):982–983. [PMC free article] [PubMed]

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