Jaffe–Campanacci syndrome explained

Synonyms:	Multiple non-ossifying fibromatosis^[1]
Jaffe–Campanacci syndrome
Field:	Medical genetics

Jaffe–Campanacci syndrome is one of the disorders associated with café au lait macules (CALMs). Presentations may include intellectual disability, disseminated non-ossifying fibromas of the long bones and jaw, hypogonadism or cryptorchidism, or giant cell granulomas of the jaw.^[2]

It was characterized in 1958 and 1983.^{[3] [4]}

See also

• List of cutaneous conditions

Notes and References

1. Web site: RESERVED . INSERM US14-- ALL RIGHTS . Orphanet: Multiple non ossifying fibromatosis . www.orpha.net . 20 April 2019 . en.
2. Book: Rapini, Ronald P. . Bolognia, Jean L. . Jorizzo, Joseph L. . Dermatology: 2-Volume Set . Mosby . St. Louis . 2007 . 831 . 978-1-4160-2999-1 .
3. 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.
4. Campanacci M, Laus M, Boriani S . Multiple non-ossifying fibromata with extraskeletal anomalies: a new syndrome? . J Bone Joint Surg Br . 65 . 5 . 627–32 . November 1983 . 6643569 . 10.1302/0301-620X.65B5.6643569.