Neurofibromatosis type I (NF-1) is a complex multi-system human disorder caused by the mutation of a gene on chromosome 17 that is responsible for production of a protein, called neurofibromin, which is needed for normal function in many human cell types.
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.
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.