Neurofibromatosis - Neurofibromatozhttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatoz (Neurofibromatosis) se yon maladi konplèks milti-sistèm imen ki te koze pa mitasyon neurofibromin. neurofibromatoz (Neurofibromatosis) lakòz timè nan sistèm nève a ki ka grandi nenpòt kote sou kò a. neurofibromatoz (Neurofibromatosis) se youn nan maladi jenetik ki pi komen ak yon maladi otozomal dominan.

Sentòm komen neurofibromatoz (Neurofibromatosis) gen ladan tach mawon-wouj nan pati ki gen koulè nan je a ki rele nodul Lisch ak neurofibromas (neurofibromas). Eskolyoz (koub kolòn vètebral la), andikap aprantisaj, twoub vizyon, andikap mantal, plizyè tach kafe au lait ak epilepsi ka akonpaye tou.

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  • Cafe au lait macule wè nan Neurofibromatosis type 1 (NF-1)
  • Plizyè neurofibroma (Multiple Neurofibromas) (maladi Von Recklinghausen (Von Recklinghausen disease))
  • neurofibwòm (Neurofibroma)
  • Plizyè ti neurofibromas.
  • NF-1 ― Dos pasyan granmoun aje.
  • Manifestasyon tipik nan NF-1. Yon kantite nerofibrom yo obsève ak pigmantasyon tachete.
  • Pasyan ki gen angiofibroma sou figi ki koze pa tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis se yon kondisyon ki lakòz timè nan sistèm nève a ak po. Kalite 1 eritye dominan epi li montre sentòm tankou neurofibromas, tach kafe‑a‑lait (café‑au‑lait spots), tache (freckling), ak glioma optik (optic gliomas). Dyagnostik la baze sou siy klinik yo. Kalite 2, nan lòt men an, make pa schwannoma vestibulè bilateral (bilateral vestibular schwannomas, VS) ak meningioma (meningiomas), tou eritye dominan. Jesyon an enplike siveyans regilye ak tretman medikal jan sa nesesè pou tou de kalite neurofibromatosis.
Neurofibromatosis is a neurocutaneous disorder characterized by tumors in the nervous system and skin. Neurofibromatosis types 1 and 2 are the most common and are distinct entities. Neurofibromatosis type 1, or von Recklinghausen disease, is an autosomal dominant disease. Neurofibromatosis type 1 presents with neurofibromas, cafe-au-lait macules, freckling, and optic gliomas. It is a clinical diagnosis. Neurofibromatosis type 2 (NF2) is a disease characterized by bilateral vestibular schwannomas (VS) and meningiomas. It has an autosomal dominant inheritance pattern. Treatment for neurofibromatosis types 1 and 2 is clinical monitoring and medical intervention when appropriate.