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.
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Cafe au lait macule lagu arkay Neurofibromatosis type 1 (NF-1)
Neurofibromatosis waa xaalad keenta burooyin ku dhaca habdhiska neerfaha iyo maqaarka. Nooca 1 aad ayaa loo kala dhaxlaa wuxuuna muujiyaa calaamadaha sida neurofibromas, café-au-lait spots, freckling, and optic gliomas. Cilad-sheegiddu waxay ku salaysan tahay calaamadaha bukaan-socodka. Nooca 2, dhinaca kale, waxaa lagu calaamadeeyay bilateral vestibular schwannomas (VS) and meningiomas , sidoo kale dhaxal ahaan inta badan. Maaraynta waxay ku lug leedahay la socodka joogtada ah iyo daawaynta daawaynta marka loo baahdo labada nooc ee 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.
Calaamadaha caadiga ah ee neurofibromatosis waxaa ka mid ah dhibco guduudan oo casaan ah oo ku yaal qaybta midabka isha ee loo yaqaanno Lisch nodules iyo neurofibromas. Scoliosis (qallooca laf dhabarta), naafonimada waxbarashada, khalkhalka aragga, itaaldarrada maskaxda, maqaaxiyo badan oo kafeega au lait spots iyo suuxdin ayaa sidoo kale la socon kara.
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