Neurofibromatosis ke bothata bo rarahaneng ba tsamaiso e mengata ea batho bo bakoang ke phetoho ea neurofibromin. Neurofibromatosis e baka lihlahala haufi le tsamaiso ea methapo e ka holang kae kapa kae 'meleng. Neurofibromatosis ke e 'ngoe ea mafu a atileng haholo a lefutso le lefu le atileng haholo la autosomal.
Matshwao a tlwaelehileng a neurofibromatosis a kenyeletsa matheba a bosootho bo bokgubedu karolong e mebala ya leihlo e bitswang Lisch nodules le neurofibromas. Scoliosis (ho kobeha ha mokokotlo), bokooa ba ho ithuta, mathata a pono, bokooa ba kelello, libaka tse ngata tsa café au lait le lefu la sethoathoa le tsona li ka tsamaea.
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.
☆ Liphethong tsa 2022 Stiftung Warentest tse tsoang Jeremane, khotsofalo ea bareki ka ModelDerm e ne e le tlase hanyane ho feta lipuisano tse lefelloang tsa telemedicine.
Cafe au lait macule e bonoa ho Neurofibromatosis type 1 (NF-1)
Neurofibromatosis ke boemo bo bakang lihlahala tsamaisong ea methapo le letlalo. Mofuta oa 1 o futsitsoe haholo 'me o bontša matšoao a kang neurofibromas, café-au-lait spots, freckling, and optic gliomas. Tlhahlobo e itšetlehile ka matšoao a kliniki. Mofuta oa 2, ka lehlakoreng le leng, o tšoailoe ka bilateral vestibular schwannomas (VS) and meningiomas , hape o futsitsoe haholo. Tsamaiso e kenyelletsa ho beha leihlo kamehla le kalafo ea bongaka ha ho hlokahala bakeng sa mefuta e 'meli ea 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.
Matshwao a tlwaelehileng a neurofibromatosis a kenyeletsa matheba a bosootho bo bokgubedu karolong e mebala ya leihlo e bitswang Lisch nodules le neurofibromas. Scoliosis (ho kobeha ha mokokotlo), bokooa ba ho ithuta, mathata a pono, bokooa ba kelello, libaka tse ngata tsa café au lait le lefu la sethoathoa le tsona li ka tsamaea.
Ha ho na phekolo e khethehileng ho fihlela joale.