منابع مشابه
A case of infantile cortical hyperostosis.
Infantile cortical hyperosteosis (ICH) is usually a self-limited disease of infancy with bony changes, soft tissue swelling, fever, irritability, decreased appetite, and decreased movement of the affected bones. Its description in isolated patients or in multiple members of families suggests the existence of two different forms, namely a sporadic form and a familial form with incomplete penetra...
متن کامل[Infantile cortical hyperostosis].
The genetic aspects of infantile cortical hyperostosis are discussed. A pedigree is presented, based on the history and clinical and radiological investigations of all living members of the family, with data from 11 cases with the condition in two generations, and one possible case from a third generation. The data suggest that an autosomal dominant gene with varying expressivity could be respo...
متن کاملInfantile cortical hyperostosis (Caffey's disease): a case report.
An infant in hospital unexpectedly developed infantile cortical hyperostosis (Caffey's disease) while under-going treatment for an unrelated illness. The presentation of the disease was classic and there was marked thrombocytosis. The aetiological possibilities are discussed.
متن کاملCaffey disease or infantile cortical hyperostosis: a case report.
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...
متن کاملInfantile cortical hyperostosis with raised immunoglobulins.
Two cases of infantile cortical hyperostosis are reported. Both had raised immunoglobulins. Particularly remarkable were the IgA and IgM levels, a finding infrequently reported.
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ژورنال
عنوان ژورنال: Journal of Nippon Medical School
سال: 2001
ISSN: 1345-4676,1347-3409
DOI: 10.1272/jnms.68.442