Neurofibromatosis - Neurofibromatoza
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U rezultatima Stiftung Warentest iz Njemačke za 2022., zadovoljstvo potrošača s ModelDermom bilo je samo malo niže nego s plaćenim konzultacijama o telemedicini.
Cafe au lait macule viđena kod Neurofibromatosis type 1 (NF‑1).
relevance score : -100.0%
ReferencesNeurofibromatoza je stanje koje uzrokuje tumore u živčanom sustavu i koži. Tip 1 nasljeđuje se dominantno i karakterizira se simptomima poput neurofibromas (neurofibroma), café‑au‑lait spots (café‑au‑lait mrlje), freckling (fleke) i optic gliomas (opticki gliomi). Tip 2, s druge strane, obilježen je bilateral vestibular schwannomas (bilateralni vestibularni schwannomi) (VS) i meningiomas (meningiomi), također nasljeđuje se dominantno. Liječenje uključuje redovito praćenje i medicinski tretman prema potrebi za obje vrste neurofibromatoze.
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.
Uobičajeni simptomi Neurofibromatoza (Neurofibromatosis) uključuju smeđe‑crvene mrlje u obojanom dijelu oka, poznate kao Lisch čvorovi, te neurofibrome. Skolioza (zakrivljenost kralježnice), poteškoće u učenju, poremećaji vida, mentalne poteškoće, višestruke mrlje tipa café‑au‑lait i epilepsija također mogu biti prisutni.
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