Campanacci, Mario

(redirected from Jaffe-Campanacci syndrome)

Campanacci,

Mario, Italian physician, 1932-1999.
Campanacci syndrome - syndrome characterized by pain, swelling, café-au-lait spots, and at times hypogonadism and developmental delay. Synonym(s): Jaffe-Campanacci syndrome
Jaffe-Campanacci syndrome - Synonym(s): Campanacci syndrome
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References in periodicals archive ?
Giant cell granuloma, hyperparathyroidism, Noonan's syndrome, Ramon syndrome, fibrous dysplasia, Jaffe-Campanacci syndrome, Neurofibromatosis type 1, and multiple odontogenic keratocysts are considered in differential diagnosis of cherubism.
Case Report of Nonfamilial Cherubism in a Toddler: Description of Clinic-Radiographic Features and Osseous-Dental Treatments
(44) A few patients with multiple NOFs are associated with "cafe-au-lait" spots on the skin, reminiscent of the stigmata of neurofibromatosis, type 1; an association known as Jaffe-Campanacci syndrome. (45,46) Both lesions are associated with actively growing long bones.
Non-ossifying fibroma, fibrous cortical defect and Jaffe-Campanacci syndrome: a biologic and clinical review.
Nonneoplastic lesions that simulate primary tumors of bone
Jaffe-Campanacci syndrome. A case report and review of the literature.
Jaffe Campanacci syndrome and non-convulsive status epilepticus: a case report /Jaffe Campanacci sendromu ve nonkonvulzif status epileptikus: bir olgu sunumu
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