Jaffe–Campanacci syndrome

Other names| Multiple non-ossifying fibromatosis[1]
Jaffe-Campanacci-Syndrome, boy 7 Y, tibial bowing and cortical/subcortial mixed sclerosis

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][5]

## See also

* List of cutaneous conditions

## References

1. ↑ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Multiple non ossifying fibromatosis" (in en). https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2029.
2. ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. pp. 831. ISBN 978-1-4160-2999-1.
3. ↑ synd/2486 at Who Named It?
4. ↑ 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.
5. ↑ "Multiple non-ossifying fibromata with extraskeletal anomalies: a new syndrome?". J Bone Joint Surg Br 65 (5): 627–32. November 1983. doi:10.1302/0301-620X.65B5.6643569. PMID 6643569.

## External links

Classification|

* ICD-10: M89.2
* DiseasesDB: 32263

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External resources|

* Orphanet: 2029

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