Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis bụ ọrịa mgbagwoju anya nke metụtara ọtụtụ sistemụ ahụ, kpatara mgbanwe na neurofibromin. Ọ na-ebute uto n’akụkụ sistemụ ụjọ, nke nwere ike ịmalite n’ebe ọ bụla n’ahụ. Neurofibromatosis bụ otu n’ime ọrịa mkpụrụ ndụ ihe nketa a na-ahụkarị, yana nsogbu autosomal.

Mgbaàmà ndị a na-ahụkarị gụnyere ntụpọ uhie na-acha aja aja n’akụkụ anya, nke a na-akpọ Lisch nodules, yana neurofibromas. Scoliosis (mkpụkọ ọkpụkpụ azụ), nkwarụ mmụta, nsogbu ịhụ ụzọ, nkwarụ uche, ọtụtụ cafe au lait spots, na epilepsy nwekwara ike ịbịa n’akụkụ ya.

Enweghị ọgwụgwọ a kapịrị ọnụ maka ya ugbu a.

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  • Cafe au lait macule a na-ahụ na Neurofibromatosis type 1 (NF-1)
  • Ọtụtụ Neurofibroma (Von Recklinghausen disease)
  • Neurofibroma
  • Enwere ọtụtụ obere neurofibromas.
  • NF-1 – onye ọrịa agadi.
  • Ngosipụta NF-1: A na-ahụ ọtụtụ neurofibromas na-acha ntụ ntụ.
  • Onye nwere ihu angiofibroma nke sitere na tuberous sclerosis.
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis bụ ọnọdụ na-ebute etuto na sistem ụjọ na akpụkpọ ahụ. A na-ekewa ụdị 1 nke ukwuu ma gosipụta mgbaàmà dịka neurofibromas, café‑au‑lait spots, freckling, na optic gliomas. Nchọpụta na-eme site n’akara ụlọ ọgwụ. Ụdị 2, n’aka nke ọzọ, bụ akara bilateral vestibular schwannomas (VS) na meningiomas, nke a na-ahụkarị nke ukwuu. Nlekọta gụnyere nlekọta oge na ọgwụgwọ kwesịrị ekwesị dịka ọ dị mkpa maka ụdị abụọ 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.