Abinun M, Mikuska M, Filipović B
Mother and Child Health Institute, Novi Beograd, Yugoslavia.
Eur J Pediatr. 1988 Jun;147(5):518-9. doi: 10.1007/BF00441979.
A case report of an infant with the Wiskott-Aldrich syndrome and clinical and radiological features of infantile cortical hyperostosis (Caffey disease) is presented. This is the third case described of the association of these two rare disorders and gives further support to the role of an immunologic defect in the pathogenesis of infantile cortical hyperostosis.
本文报告了一例患有维斯科特-奥尔德里奇综合征且具有婴儿皮质增生症(卡菲病)临床和放射学特征的婴儿病例。这是描述的这两种罕见疾病关联的第三例病例,进一步支持了免疫缺陷在婴儿皮质增生症发病机制中的作用。