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 enye 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. 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.

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  • 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.