Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis ke bothata bo rarahaneng ba tsamaiso e mengata ea motho bo bakwang ke phetoho ea neurofibromin. Neurofibromatosis e baka lihlahala haufi le tsamaiso ea methapo e ka holang 'meleng. Neurofibromatosis ke e 'ngoe ea mafu a atileng haholo a lefutso le a atileng haholo a autosomal.

Matshwao a tlwaelehileng a neurofibromatosis a kenyelletsa matheba a bosootho bo bokgobodu karolong e mebala ea leihlo e bitswang Lisch nodules le neurofibromas. Scoliosis (ho kobeha ha mokokotlo), bokooa ba ho ithuta, mathata a pono, bokooa ba kelello, libaka tse ngata tsa café au lait, le lefu la sethoathoa li ka tsamaea.

Ha ho na phekolo e khethehileng ho fihlela joale.

☆ AI Dermatology — Free Service
Liphethong tsa 2022 Stiftung Warentest tse tsoang Jeremane, khotsofalo ea bareki ka ModelDerm e ne e le tlase hanyane ho feta lipuisano tse lefelloang tsa telemedicine.
  • Cafe au lait macule e bonoa ho Neurofibromatosis type 1 (NF-1).
  • Multiple neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Li-neurofibroma tse ngata, tse nyane.
  • NF-1 ― Mokokotlo oa mokuli o tsofetseng.
  • Pontšo e tloaelehileng ea NF-1. Li-neurofibromas tse ngata li bonahala ka mebala e fapaneng.
  • Mokuli o nang le angiofibroma ea sefahleho e bakwang ke tuberous sclerosis.
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis ke boemo bo bakang lihlahala tsamaisong ea methapo le letlalo. Mofuta oa 1 o bont'oa haholo 'me o na le matšoao a kang neurofibromas, café‑au‑lait spots, freckling, le optic gliomas. Tlhahlobo e itšetlehile ka matšoao a kliniki. Mofuta oa 2, ka lehlakoreng le leng, o tšoana le bilateral vestibular schwannomas (VS) le meningiomas, hape o bont'oa haholo. Tsamaiso e kenyelletsa ho beha leihlo kamehla le kalafo ea bongaka ha ho hlokahala bakeng sa mefuta e 'meli ea 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.