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 nodil Lisch ak nerofibrom. Eskolyoz (kob kolòn vètebral la), andikap aprantisaj, twoub vizyon, andikap mantal, plizyè tach kafe au lait ak epilepsi ka akonpaye tou.

Pa gen okenn tretman espesifik kòm nan ankò.

☆ Nan rezilta Stiftung Warentest 2022 ki soti nan Almay, satisfaksyon konsomatè yo ak ModelDerm te sèlman yon ti kras pi ba pase ak konsiltasyon telemedsin peye.
  • Cafe au lait macule wè nan Neurofibromatosis type 1 (NF-1)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Plizyè ti neurofibromas.
  • NF-1 ― Do pasyan granmoun aje.
  • Manifestasyon tipik nan NF-1. Yon kantite nerofibrom yo obsève ak pigmantasyon tachete.
  • Pasyan ak vizaj angiofibroma ki te koze pa tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis se yon kondisyon ki lakòz timè nan sistèm nève a ak po. Kalite 1 eritye dominantman epi li montre sentòm tankou neurofibromas, café-au-lait spots, freckling, and optic gliomas. Dyagnostik la baze sou siy klinik yo. Kalite 2, nan lòt men an, make pa bilateral vestibular schwannomas (VS) and meningiomas , tou eritye dominantman. Jesyon 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.