Caffey disease or infantile cortical hyperostosis: a case report.
نویسندگان
چکیده
Caffey disease or Infantile Cortical Hyperostosis (ICH) is a rare and mostly self limiting condition affecting young infants. It is characterized by acute inflammation of the periostium and the overlying soft tissue and is accompanied by systemic changes of irritability and fever. Diagnosis may be delayed as this disorder mimics a wide range of diseases including osteomyelitis, hypervitaminosis A, scurvy, bone tumors and child abuse. The emphasis here is to remind clinicians about the existence of the disease in this country.
منابع مشابه
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1 Caffey J, Silverman W. Infantile cortical hyperostosis. Preliminary report in a new syndrome. AJR 1945;54:1. 2 Van Buskirk FW, Tampas JP, Peterson OS Jr. Infantile cortical hyperostosis. An enquiry into its familial aspects. AJR 1961;85:613. 3 Finsterbush A, Rang M. Infantile cortical hyperostosis. Followup of 29 cases. Acta Orthop Scand 1975;46:727. 4 Jackson DR, Lyne ED. Infantile cortical ...
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A particular mutation in the COL1A1 gene causes infantile cortical hyperostosis, commonly known as Caffey disease. The signs and symptoms of Caffey disease are usually apparent by the time an infant is 5 months old. This condition is characterized by swelling of soft tissues (muscles, for example), pain, and excessive new bone formation (hyperostosis). The bone abnormalities mainly affect the j...
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ورودعنوان ژورنال:
- Oman medical journal
دوره 25 2 شماره
صفحات -
تاریخ انتشار 2010