Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis bụ ihe mgbagwoju anya ọtụtụ sistemu mmadụ kpatara ngbanwe nke neurofibromin. Neurofibromatosis na-ebute etuto n'akụkụ sistemu ụjọ nke nwere ike itolite n'ebe ọ bụla na ahụ. Neurofibromatosis bụ otu n'ime ọrịa mkpụrụ ndụ ihe nketa a na-ahụkarị yana nsogbu nke autosomal.

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

Enweghị ọgwụgwọ a kapịrị ọnụ ka ọ dị ugbu a.

☆ Na nsonaazụ Stiftung Warentest nke 2022 sitere na Germany, afọ ojuju ndị ahịa na ModelDerm dị ntakịrị ntakịrị karịa na nyocha telemedicine akwụ ụgwọ.
  • Cafe au lait macule hụrụ na Neurofibromatosis type 1 (NF-1)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Ọtụtụ obere neurofibromas.
  • NF-1 - azụ onye ọrịa agadi.
  • Ngosipụta nke NF-1. A na-ahụ ọtụtụ neurofibromas na-acha ntụ ntụ.
  • Onye nwere ihu angiofibroma butere tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis bụ ọnọdụ na-ebute etuto na sistem ụjọ na akpụkpọ ahụ. A na-eketa ụdị 1 nke ukwuu ma gosipụta mgbaàmà dịka neurofibromas, café-au-lait spots, freckling, and optic gliomas. Nchọpụta nyocha dabere na akara ụlọ ọgwụ. Ụdị 2, n'aka nke ọzọ, bụ akara bilateral vestibular schwannomas (VS) and meningiomas , nke eketakwara nke ukwuu. Nlekọta gụnyere nlekota oge na ọgwụgwọ ahụike 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.