Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis ose fa'alavelave fa'alavelave fa'aletonu o tagata e mafua mai i suiga ole neurofibromin. Neurofibromatosis e mafua ai tuma i luga o le neura e mafai ona tupu i soo se mea i le tino. Neurofibromatosis ose tasi o fa'afitauli masani fa'atupu ma se fa'aletonu o le autosomal dominant.

O fa'ailoga masani ole neurofibromatosis e aofia ai ma'ila lanu enaena-mumu i le vaega lanu o le mata e ta'ua o Lisch nodules ma neurofibromas. Scoliosis (curvature of the spine), fa'aletonu le a'oa'oina, fa'aletonu le va'ai, fa'aletonu le mafaufau, tele café au lait spots ma epilepsy e mafai fo'i ona fa'atasi.

E leai se togafitiga faʻapitoa i le taimi nei.

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  • Cafe au lait macule vaaia i Neurofibromatosis type 1 (NF-1)
  • Neurofibroma tele (Multiple Neurofibromas) (Von Recklinghausen disease)
  • Neurofibroma
  • Neurofibromatosis (Neurofibromatosis)
  • NF-1 ― Tua o tagata ma‘i matutua.
  • Fa'aaliga masani o le NF-1. O le tele o neurofibromas o lo'o mata'itu i le fa'ailoga lanu.
  • Tagata ma'i i le foliga angiofibroma mafua mai le tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis o se tulaga e mafua ai le tuma i le tino ma le paʻu. O le ituaiga 1 fa'amaonia ma fa'aalia fa'ailoga pei o neurofibromas, café‑au‑lait spots, freckling, ma optic gliomas. E fa'avae su'esu'ega i le fa'ailoga i le falema'i. O le ituaiga 2, i le isi itu, ua faailogaina i le bilateral vestibular schwannomas (VS) ma meningiomas, fa'amaonia. O le pulega e aofia ai le mata'ituina masani ma togafitiga fa'afoma'i pe a mana'omia mo ituaiga uma e lua o 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.