- Jaffe–Campanacci syndrome
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Jaffe–Campanacci syndrome Classification and external resources DiseasesDB 32263 Jaffe–Campanacci syndrome is one of the disorders associated with café au lait macules (CALMs). Presentations may include mental retardation, disseminated non-ossifying fibromas of the long bones and jaw, hypogonadism or cryptorchidism, or giant cell granulomas of the jaw.[1]
It was characterized in 1958 and 1983.[2][3][4]
See also
References
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. pp. 831. ISBN 1-4160-2999-0.
- ^ synd/2486 at Who Named It?
- ^ H. L. Jaffe.Non-ossifying fibromata. In: H. L. Jaffe, editor: Tumors and Tumorous Conditions of the Bones and Joints. Philadelphia, Lea & Febiger, 1958, pp 117-141.
- ^ Campanacci M, Laus M, Boriani S (November 1983). "Multiple non-ossifying fibromata with extraskeletal anomalies: a new syndrome?". J Bone Joint Surg Br 65 (5): 627–32. PMID 6643569. http://www.jbjs.org.uk/cgi/pmidlookup?view=long&pmid=6643569.
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