Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis cuta ce mai rikitarwa ta tsarin ɗan adam wanda ke haifar da canje‑canje a cikin gen ɗin neurofibromin. Neurofibromatosis yana haifar da tumori a cikin tsarin jijiyoyi wanda zai iya girma a ko'ina a jiki. Neurofibromatosis yana ɗaya daga cikin cututtukan gado na kwayoyin halitta mafi yawan samu kuma yana bin tsarin gado na autosomal dominant.

Alamomi na yau da kullun na neurofibromatosis sun haɗa da tabo mai launin ruwan kasa‑ja a cikin ido da ake kira Lisch nodules da neurofibromas. Scoliosis (curvature na kashin baya), nakasar ilmantarwa, matsalar hangen nesa, nakasar tunani, tabo da yawa na café au lait, da cutar epilepsy.

Babu takamaiman magani har yanzu.

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  • Yawanci alamu sun haɗa da Neurofibromatosis type 1 (NF-1).
  • Neurofibromas da yawa (Von Recklinghausen disease)
  • Neurofibroma
  • Ƙananan neurofibromas da yawa.
  • NF-1 ― Baya na maras lafiya tsoho.
  • Alamar bayyanar NF-1. Ana lura da adadin neurofibromas tare da ƙwanƙolin launi.
  • Mai haƙuri da angiofibroma na fuska da aka haifar da tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis cuta ce da ke haifar da ciwace-ciwace a cikin tsarin jijiya da fata. Nau'in 1 ana gado ne sosai kuma yana nuna alamun kamar neurofibromas, café-au-lait spots, freckling, and optic gliomas. Gano ganewar asali yana dogara ne akan alamun asibiti. Nau'in 2, a daya bangaren, yana da alamar bilateral vestibular schwannomas (VS) and meningiomas, wanda ma ke da gado na autosomal dominant. Gudanarwa ya ƙunshi saka idanu akai-akai da magani kamar yadda ake buƙata don nau'ikan 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.