Neurofibromatosis - Neurofibromatoza
☆ 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 viđeno u Neurofibromatosis type 1 (NF-1)
References
Neurofibromatosis je stanje koje uzrokuje tumore u živčanom sustavu i koži. Tip 1 se nasljeđuje dominantno i pokazuje simptome poput neurofibromas, café-au-lait spots, freckling, and optic gliomas. Dijagnoza se postavlja na temelju kliničkih znakova. Tip 2, s druge strane, obilježen je s bilateral vestibular schwannomas (VS) and meningiomas , također se nasljeđuje dominantno. Liječenje uključuje redovito praćenje i medicinski tretman prema potrebi za obje vrste 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.
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 obojenom dijelu oka koje se nazivaju Lisch čvorovi i neurofibromi. Skolioza (zakrivljenost kralježnice), poteškoće u učenju, poremećaji vida, mentalne poteškoće, višestruke mrlje od café au lait i epilepsija također mogu biti popraćeni.
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