Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
I- Neurofibromatosis yinkqubo entsonkothileyo yokuphazamiseka komntu okubangelwa kukuguqulwa kwe-neurofibromin. Neurofibromatosis ibangela amathumba ecaleni kwenkqubo yemithambo-luvo enokukhula naphi na emzimbeni. I- neurofibromatosis yenye yezona zifo zixhaphakileyo zemfuzo kunye ne-autosomal dominant disorder.

Iimpawu eziqhelekileyo ze- neurofibromatosis ziquka amabala amdaka-bomvu kwindawo enemibala yeliso ebizwa ngokuba yi-Lisch nodules kunye ne-neurofibromas. I-Scoliosis (i-curvature of the spine), ukukhubazeka kokufunda, ukuphazamiseka kokubona, ukukhubazeka kwengqondo, iindawo ezininzi ze-café au lait kunye nokuxhuzula kunokukhatshwa.

Akukho nyango lukhethekileyo okwangoku.

☆ Kwiziphumo zika-2022 ze-Stiftung Warentest ezivela eJamani, ukwaneliseka kwabathengi ngeModelDerm bekungaphantsi kancinci kunokubonisana nge-telemedicine ehlawulweyo.
  • Cafe au lait macule ibonwe kwi Neurofibromatosis type 1 (NF-1)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Iineurofibromas ezininzi ezincinci.
  • NF-1 ― Umqolo wesigulana esikhulileyo.
  • Ubonakaliso oluqhelekileyo lwe-NF-1. Inani lee-neurofibromas lijongwa ngebala elinamachokoza.
  • Isigulana sobuso angiofibroma sibangelwa tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis yimeko ebangela amathumba kwi-nervous system kunye nolusu. Udidi loku-1 lufuzwe kakhulu kwaye lubonisa iimpawu ezinje nge neurofibromas, café-au-lait spots, freckling, and optic gliomas. Ukuxilongwa kusekelwe kwiimpawu zeklinikhi. Udidi lwesi-2, kwelinye icala, luphawulwe ngo bilateral vestibular schwannomas (VS) and meningiomas , nalo lizuzwe kakhulu. Ulawulo lubandakanya ukubekwa kweliso rhoqo kunye nonyango lwezonyango njengoko lufuneka kuzo zombini iindidi ze 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.