Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis yakaoma multi-system human disorder inokonzerwa nekuchinja kwe neurofibromin. Neurofibromatosis inokonzeresa mapundi pamwe chete netsinga dzetsinga dzinogona kukura chero pamuviri. Neurofibromatosis ndeimwe yeanowanzo zivikanwa genetic kusagadzikana uye autosomal dominant disorder.

Zviratidzo zvinowanzoonekwa zve neurofibromatosis zvinosanganisira mavara matsvuku‑tsvuku muchikamu cheziso chinonzi Lisch nodules uye neurofibromas. Scoliosis (kukombama kwemusana), kurema kwekudzidza (learning difficulties), kusaona zvakanaka (visual problems), kurema kwepfungwa (intellectual disability), nzvimbo dzakawanda dze café au lait (café au lait spots) zvinogona kuperekedzwawo.

Hakusati kwave nemabatirwo chaiwo.

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  • Cafe au lait macule yaonekwa muNeurofibromatosis type 1 (NF-1)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Multiple diki neurofibromas.
  • NF-1 ― Murwere akura musana.
  • Yakajairika kuratidzwa kweNF-1. Nhamba ye neurofibromas inocherechedzwa ine mavara ane mavara.
  • Murwere ane chiso angiofibroma zvichikonzerwa netuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis is a condition inokonzera mapundi mutsanga dzetsinga neganda. Type 1 inogarwa nhaka zvakanyanya uye inoratidza zviratidzo se neurofibromas, café-au-lait spots, freckling, and optic gliomas. Kuongororwa kunobva pane zviratidzo zvekliniki. Type 2, kune rumwe rutivi, inomikwa ne bilateral vestibular schwannomas (VS) and meningiomas , zvakare yakagarwa nhaka zvakanyanya. Kutungamira kunosanganisira kugara uchitarisa uye kurapwa sezvinodiwa kune ese marudzi e 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.