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Jaffe–Campanacci syndrome

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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]

Other namesMultiple non-ossifying fibromatosis[1]
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Jaffe–Campanacci syndrome
Other namesMultiple non-ossifying fibromatosis[1]
Jaffe-Campanacci-Syndrome, boy 7 Y, tibial bowing and cortical/subcortial mixed sclerosis
SpecialtyMedical genetics
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It was characterized in 1958 and 1983.[3][4][5]

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