Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis ndizovuta zamitundumitundu zamunthu zomwe zimachitika chifukwa cha kusintha kwa neurofibromin. Neurofibromatosis imayambitsa zotupa m'mitsempha yamanjenje zomwe zimatha kukula kulikonse mthupi. Neurofibromatosis ndi imodzi mwazovuta zofala kwambiri za majini komanso vuto lalikulu la autosomal.

Zizindikiro zodziwika bwino za neurofibromatosis zimaphatikizira mawanga ofiira abulauni pagawo lakuda la diso lotchedwa Lisch nodules ndi neurofibromas. Scoliosis (kupindika kwa msana), kulephera kuphunzira, kusokonezeka kwa masomphenya, kulumala kwamaganizidwe, ma café au lait spots angapo komanso khunyu.

Palibe chithandizo chenichenicho mpaka pano.

☆ Muzotsatira za 2022 Stiftung Warentest zochokera ku Germany, kukhutitsidwa kwa ogula ndi ModelDerm kunali kotsika pang'ono kusiyana ndi kuyankhulana kwa telemedicine komwe kulipiridwa.
  • Cafe au lait macule zowoneka mu Neurofibromatosis type 1 (NF-1)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Ma neurofibromas angapo ang'onoang'ono.
  • NF-1 ― Wodwala okalamba kumbuyo.
  • Chiwonetsero chodziwika bwino cha NF-1. Ma neurofibromas angapo amawonedwa ndi utoto wamawanga.
  • Wodwala wa nkhope angiofibroma chifukwa cha tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis ndi vuto lomwe limayambitsa zotupa mu dongosolo lamanjenje ndi khungu. Mtundu 1 umakhala wotengera kwambiri ndipo umasonyeza zizindikiro monga neurofibromas, café-au-lait spots, freckling, and optic gliomas. Matendawa amatengera zizindikiro zachipatala. Type 2, kumbali ina, imalembedwa ndi bilateral vestibular schwannomas (VS) and meningiomas , yomwe imatengeranso cholowa kwambiri. Kuyang'anira kumaphatikizapo kuyang'anira nthawi zonse ndi chithandizo chamankhwala monga kufunikira pamitundu yonse ya 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.