Neurofibromatosis - Neurofibromatosia
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Cafe au lait macule Neurofibromatosis type 1 (NF-1)-n ikusia
References
Neurofibromatosis nerbio-sisteman eta larruazalean tumoreak eragiten dituen egoera da. 1 mota nagusiki heredatzen da eta neurofibromas, café-au-lait spots, freckling, and optic gliomas bezalako sintomak erakusten ditu. Diagnostikoa seinale klinikoetan oinarritzen da. 2. Mota, berriz, bilateral vestibular schwannomas (VS) and meningiomas markatuta dago, oinordetzan ere nagusiki. Kudeaketak erregular kontrola eta tratamendu medikoa dakar bi motatako neurofibromatosis behar den moduan.
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.
neurofibromatosia (neurofibromatosis) ren sintomak ohikoak dira Lisch-ko noduluak eta neurofibromak izeneko begiaren koloreko zatian dauden orban marroi-gorriak. Eskoliosia (bizkarrezurreko kurbatura), ikaskuntza-urritasunak, ikusmen-nahasteak, buru-urritasunak, hainbat kafe au lait leku eta epilepsia ere egon daitezke.
Oraindik ez dago tratamendu zehatzik.