Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis o se fa'alavelave fa'alavelave fa'aletonu o tagata e mafua mai i suiga i le neurofibromin. Neurofibromatosis e mafua ai tuma i le nervous system e mafai ona tupu i soo se vaega o le tino. Neurofibromatosis o se tasi o fa'afitauli masani ma le autosomal dominant inheritance pattern.

O fa'ailoga masani o le neurofibromatosis e aofia ai ma'ila lanu enaena‑mumu (brown‑red spots) i le iris (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)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Tele neurofibromas laiti.
  • NF-1 ― Tua o tagata ma‘i matutua.
  • Fa'aaliga masani o le NF-1. O le tele o neurofibromas o loʻo matauina i le faʻailoga lanu.
  • Tagata ma'i i foliga angiofibroma mafua mai tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis ose tulaga e mafua ai le tuma i le tino ma le paʻu. O le ituaiga 1 e fa'ama'i autosomal ma fa'aalia fa'ailoga pei o neurofibroma (neurofibromas), poka café‑au‑lait (café‑au‑lait spots), puka (freckling) ma glioma o le mata (optic gliomas). E fa'avae su'esu'ega i fa'ailoga i le foma'i. O le ituaiga 2, i le isi itu, ua fa'ailoa i le schwannoma vestibular bilateral (bilateral vestibular schwannomas) ma meningioma (meningiomas), fa'ama'i autosomal. 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 le 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.