Neurofibromatosis - Neurofibromatosia
☆ Alemaniako Stiftung Warentest-en 2022ko emaitzetan, ModelDerm-ekin kontsumitzaileen gogobetetasuna apur bat txikiagoa izan zen ordaindutako telemedikuntzako kontsultekin baino.
Cafe au lait macule Neurofibromatosis type 1 (NF-1)-n ikusia
relevance score : -100.0%
ReferencesNeurofibromatosis nerbio-sisteman eta larruazalean tumoreak eragiten dituen egoera da. Mota nagusi bat heredatzen da eta neurofibroma, café‑au‑lait spots, freckling eta optic glioma bezalako sintomak erakusten ditu. Diagnostikoa seinale klinikoetan oinarritzen da. Bigarren mota, berriz, bilateral vestibular schwannomas (VS) eta meningioma markatuta dago, oinordetzan ere nagusiki. Kudeaketak kontrol erregularra eta tratamendu medikoa dakar bi neurofibromatosi mota 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 ohikoenak 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 ager daitezke.
Oraindik ez dago tratamendu zehatzik.