About: Jaffe–Campanacci syndrome     Goto   Sponge   NotDistinct   Permalink

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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. It was characterized in 1958 and 1983.

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  • Jaffé-Campanacci-Syndrom (de)
  • Jaffe–Campanacci syndrome (en)
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  • Das Jaffé-Campanacci-Syndrom ist eine umschriebene Dysplasie der Tibia. Beschrieben wurde sie von Henry Lewis Jaffe und Louis Lichtenstein (1942) und Mario Campanacci. (de)
  • 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. It was characterized in 1958 and 1983. (en)
foaf:name
  • Jaffe–Campanacci syndrome (en)
name
  • Jaffe–Campanacci syndrome (en)
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  • http://commons.wikimedia.org/wiki/Special:FilePath/Camp_7J.png
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DiseasesDB
ICD
  • M89.2 (en)
Orphanet
caption
  • Jaffe-Campanacci-Syndrome, boy 7 Y, tibial bowing and cortical/subcortial mixed sclerosis (en)
synonyms
  • Multiple non-ossifying fibromatosis (en)
has abstract
  • Das Jaffé-Campanacci-Syndrom ist eine umschriebene Dysplasie der Tibia. Beschrieben wurde sie von Henry Lewis Jaffe und Louis Lichtenstein (1942) und Mario Campanacci. (de)
  • 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. It was characterized in 1958 and 1983. (en)
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DiseasesDB
  • 32263
ICD10
  • M89.2
ORPHA
  • 2029
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