Neurofibromatosis - Neurofibromatoza
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U rezultatima Stiftung Warentest-a za 2022. iz Njemačke, zadovoljstvo potrošača ModelDerm-om bilo je samo nešto niže nego s plaćenim telemedicinskim konsultacijama.
U rezultatima Stiftung Warentest-a za 2022. iz Njemačke, zadovoljstvo potrošača ModelDerm-om bilo je samo nešto niže nego s plaćenim telemedicinskim konsultacijama.
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 se nasljeđuje dominantno i pokazuje simptome poput neurofibromas, café‑au‑lait spots, freckling i optic gliomas. Dijagnoza se zasniva na kliničkim znakovima. Tip 2 je, s druge strane, označen bilateralnim vestibular schwannomas (VS) i meningiomas, također dominantno naslijeđen. Upravljanje uključuje redovno praćenje i medicinski tretman prema potrebi za oba tipa 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 neurofibromatoze (Neurofibromatosis) uključuju smeđe‑crvene mrlje u očnom bjeloočku, poznate kao Lischovi čvorovi, te neurofibrome. Skolioza (zakrivljenost kičme), poteškoće u učenju, poremećaji vida, mentalne smetnje, višestruke café‑au‑lait mrlje i epilepsija također mogu biti prisutni.
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