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Page 1
A Rare Case of Lethal Prenatal-Onset Infantile Cortical Hyperostosis.
Kim ST, Kim H, Kim HH, Lee NH, Han Y, Sung SI, Chang YS, Park WS. Kim ST, et al. Yonsei Med J. 2019 May;60(5):484-486. doi: 10.3349/ymj.2019.60.5.484. Yonsei Med J. 2019. PMID: 31016912 Free PMC article.
Infantile cortical hyperostosis, or Caffey's disease, usually presents with typical radiological features of soft tissue swelling and cortical thickening of the underlying bone. ...This paper is unique in that it is the first paper to report a lethal form of
Infantile cortical hyperostosis, or Caffey's disease, usually presents with typical radiological features of soft tissu
Caffey's disease in an infant.
Raza AB, Ijaz I, Naz F, Butt TA. Raza AB, et al. J Coll Physicians Surg Pak. 2011 Oct;21(10):634-6. doi: 10.2011/JCPSP.634636. J Coll Physicians Surg Pak. 2011. PMID: 22015129
Caffey's disease is a self limited disorder of infantile age group. It is synonymous with 'infantile cortical hyperostosis' and 'Caffey's-Silver syndrome'.It is characterized by fever, irritability, bone pain and characteristic bony changes. ...
Caffey's disease is a self limited disorder of infantile age group. It is synonymous with 'infantile cortical hyperostosis
Infantile cortical hyperostosis.
Rao PT, Sahoo J. Rao PT, et al. J Indian Med Assoc. 1985 May;83(5):164-5. J Indian Med Assoc. 1985. PMID: 3902982 No abstract available.
Familial infantile cortical hyperostosis: an update.
Newberg AH, Tampas JP. Newberg AH, et al. AJR Am J Roentgenol. 1981 Jul;137(1):93-6. doi: 10.2214/ajr.137.1.93. AJR Am J Roentgenol. 1981. PMID: 6787897
In 1961, the senior author reported 11 members of one family with infantile cortical hyperostosis. Since then, 10 new cases have occurred in this family resulting in a total of 21 cases. The incidence of infantile cortical hyperostosis in …
In 1961, the senior author reported 11 members of one family with infantile cortical hyperostosis. Since then, 10 new c …
Severe prenatal infantile cortical hyperostosis (Caffey's disease).
Turnpenny PD, Davidson R, Stockdale EJ, Tolmie JL, Sutton AM. Turnpenny PD, et al. Clin Dysmorphol. 1993 Jan;2(1):81-6. Clin Dysmorphol. 1993. PMID: 8298744 Review.
We describe three cases of prenatal infantile cortical hyperostosis (Caffey's disease) from two families, all associated with maternal polyhydramnios. ...
We describe three cases of prenatal infantile cortical hyperostosis (Caffey's disease) from two families, all associate …
Infantile cortical hyperostosis. Follow-up of 29 cases.
Finsterbush A, Rang M. Finsterbush A, et al. Acta Orthop Scand. 1975 Nov;46(5):727-36. doi: 10.3109/17453677508989258. Acta Orthop Scand. 1975. PMID: 1106113
Twenty-nine cases of infantile cortical hyperostosis with a wide range of bone involvement are reviewed. ...Differential diagnosis and possible etiological factors are discussed. The similarity of infantile cortical hyperostosis to extrem …
Twenty-nine cases of infantile cortical hyperostosis with a wide range of bone involvement are reviewed. ...Differentia …
Garré's osteomyelitis of the mandible. Report of a case.
Ellis DJ, Winslow JR, Indovina AA. Ellis DJ, et al. Oral Surg Oral Med Oral Pathol. 1977 Aug;44(2):183-9. doi: 10.1016/0030-4220(77)90266-3. Oral Surg Oral Med Oral Pathol. 1977. PMID: 268570
The prognosis in cases of Ewing's sarcoma is poor, and death may occur in a matter of weeks. 2. Infantile cortical hyperostosis (Caffey's disease), which is characterized by development of soft-tissue swelling and cortical thickening of the mandible. ...
The prognosis in cases of Ewing's sarcoma is poor, and death may occur in a matter of weeks. 2. Infantile cortical hyperost
13 results