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Infantile Cortical Hyperostosis
JAMA, 1961Infantile cortical hyperostosis was first described and named by Caffey and Silverman in 1945.4Smyth, Potter, and Silverman12described a similar group of cases in a separate and independent report the next year. These reports stimulated a great deal of interest in the disease, and by 1952 there were over 100 case reports in the literature.
J P, TAMPAS +3 more
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Infantile cortical hyperostosis
Oral Surgery, Oral Medicine, Oral Pathology, 1958Abstract Swelling of the face and mandibular bone changes are of concern to the dental profession. These changes are the most frequent findings in infantile cortical hyperostosis. Although there are more than eighty cases reported in the pediatric and radiologic literature, there are no known previous reports in the dental literature.
H C, THOMPSON, J A, TABRIS
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Prenatal Cortical Hyperostosis
The British Journal of Radiology, 1953A case is described in which the features of infantile cortical hyperostosis were demonstrated radiologically, in utero. The foetus was stillborn and autopsy shed no light on the causation of the condition. That a hormonal imbalance might have an effect on bone production is put forward as a possible consideration.
H S, BENNETT, T R, NELSON
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Hyperostosis Frontalis Interna
Archives of Neurology, 2006AN 85-YEAR-OLD womanunderwenta headmagneticresonance imaging scan forevaluationofprogressive gait difficulty and memory decline. Her examination findings showedmarkedshort-termmemory problems and postural instability withmildextrapyramidalsigns.She had a history of chronic hypertension but no history of any endocrinopathy.
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Infantile cortical hyperostosis
The Journal of Pediatrics, 1956Summary A description of the clinical picture, laboratory findings, differential diagnosis, etiology, therapy, and prognosis of infantile cortical hyperostosis, with a review of the literature, is presented. Eleven new cases of infantile cortical hyperostosis are reported. Four of this series occurred in Negro infants.
F, BROOKSALER, J E, MILLER
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Cranial Hyperostosis (Hyperostosis Cranii or H.C.)
JAMA, 1964Perou has blended his own observations with those of many predecessors to emphasize the importance of the various cranial hyperostoses. A section on classification is followed by chapters on racial and hereditary pathological conditions associated with hyperostosis.
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[Vertebral hyperostosis and hyperostosis frontalis interna].
Revue du rhumatisme et des maladies osteo-articulaires, 1985Routine roentgenographic examination of the spine was performed in 690 patients with rheumatologic disorders. Ankylosing hyperostosis was discovered in 124 patients (18 percent). Roentgenograms of the skull revealed hyperostosis frontalis interna in 63 percent of cases, especially in female patients.
A, Ciocci, L, Buratti, G, Maurelli
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Neonatal Cortical Hyperostosis
Neonatal Network, 2000PROSTAGLANDIN THERAPY FOR neonates with ductal-dependent heart defects is a lifesaving intervention that permits optimal stabilization, diagnostic imaging, and timing of surgery. However, this therapy is not without complications (Table 1).1–3 When longterm (weeks or months) prostaglandin therapy is required because of neonatal immaturity or for ...
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