Neurofibromatosis - Neyrofibromatoz
☆ Germaniyaning 2022 yilgi Stiftung Warentest natijalariga ko'ra, iste'molchilarning ModelDermdan qoniqish darajasi pullik teletibbiyot maslahatlariga qaraganda bir oz pastroq bo'lgan.
Cafe au lait macule Neurofibromatosis type 1 (NF-1) da ko'rilgan
References
Neurofibromatosis - asab tizimi va terida shish paydo bo'lishiga olib keladigan holat. 1-toifa dominant tarzda meros bo'lib, neurofibromas, café-au-lait spots, freckling, and optic gliomas kabi alomatlarni ko'rsatadi. Tashxis klinik belgilarga asoslanadi. Boshqa tomondan, 2-tur bilateral vestibular schwannomas (VS) and meningiomas bilan belgilanadi, shuningdek, dominant tarzda meros qilib olinadi. Boshqaruv har ikki turdagi neurofibromatosis uchun zarur bo'lganda muntazam monitoring va tibbiy davolanishni o'z ichiga oladi.
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.
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.
neyrofibromatoz (neurofibromatosis) ning umumiy belgilari orasida Lisch tugunlari va neyrofibromalar deb ataladigan ko'zning rangli qismida jigarrang-qizil dog'lar mavjud. Skolioz (umurtqa pog'onasi egriligi), o'rganishdagi nuqsonlar, ko'rishning buzilishi, aqliy nuqsonlar, ko'plab kafe au lait dog'lari va epilepsiya hamroh bo'lishi mumkin.
Hozircha o'ziga xos davolash mavjud emas.