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neurofibromatosis

[ noor-oh-fahy-broh-muh-toh-sis, nyoor- ]

noun

, Pathology.
  1. a dominantly inherited genetic disorder characterized by flat brown patches on the skin, neurofibromas of the skin and internal organs, and in some cases skeletal deformity.


neurofibromatosis

/ ˌnjʊərəʊˌfaɪbrəməˈtəʊsɪs /

noun

  1. a condition characterized by the formation of benign tumours on the fibrous coverings of the peripheral nerves and the development of areas of café-au-lait spots
“Collins English Dictionary — Complete & Unabridged” 2012 Digital Edition © William Collins Sons & Co. Ltd. 1979, 1986 © HarperCollins Publishers 1998, 2000, 2003, 2005, 2006, 2007, 2009, 2012


neurofibromatosis

/ nr′ō-fī′brō-mə-tōsĭs /

  1. A genetic disease characterized by multiple benign tumors of peripheral nerves, called neurofibromas , and pigmented spots on the skin, sometimes accompanied by bone deformity and a predisposition to cancers, especially of the brain.


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Word History and Origins

Origin of neurofibromatosis1

1895–1900; < New Latin neurofibromat-, stem of neurofibroma neurofibroma + -osis
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Example Sentences

The scenes between Johansson and Adam Pearson, a man with neurofibromatosis, are some of the most delicate and visceral this year.

I recall being taught during my medical education that a likely diagnosis was neurofibromatosis type 1.

"Rhincho-spasm," a snoring tic, has been observed by Oppenheim in a case of neurofibromatosis.

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neurofibromaneurogenic