Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis cuta ce mai rikitarwa ta tsarin ɗan adam wanda ke haifar da maye gurbin neurofibromin. Neurofibromatosis yana haifar da ciwace-ciwace tare da tsarin juyayi wanda zai iya girma a ko'ina a jiki. Neurofibromatosis yana ɗaya daga cikin cututtukan ƙwayoyin cuta na yau da kullun da kuma rashin ƙarfi na autosomal.

Alamomi na yau da kullun na neurofibromatosis sun haɗa da tabo mai launin ruwan kasa-ja a cikin ɓangaren ido masu launin Lisch nodules da neurofibromas. Scoliosis (curvature na kashin baya), nakasar ilmantarwa, matsalar hangen nesa, nakasar tunani, cafe da yawa au lait spots da farfadiya kuma na iya kasancewa tare.

Babu takamaiman magani har yanzu.

☆ A cikin sakamakon Stiftung Warentest na 2022 daga Jamus, gamsuwar mabukaci tare da ModelDerm ya ɗan yi ƙasa kaɗan fiye da biyan shawarwarin telemedicine.
  • yawanci ana lura dashi a Neurofibromatosis type 1 (NF-1).
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Ƙananan ƙananan neurofibromas.
  • NF-1 ― Mara lafiyar tsofaffi.
  • Alamar bayyanar NF-1. Ana lura da adadin neurofibromas tare da ƙwanƙolin launi.
  • Mai haƙuri da fuska angiofibroma ya 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 nau'in 2, a daya bangaren, yana da alamar bilateral vestibular schwannomas (VS) and meningiomas , wanda kuma aka yi gadon rinjaye. 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.