Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis yaiku kelainan multi‑sistem sing kompleks lan disebabake dening mutasi neurofibromin. Neurofibromatosis nyebabake tumor ing sistem saraf sing bisa tuwuh ing endi wae ing awak. Neurofibromatosis minangka salah sawijining kelainan genetik sing paling umum lan kelainan autosomal dominan.

Gejala sing umum saka neurofibromatosis kalebu bintik‑bintik abang‑coklat ing bagian mripat sing diarani nodul Lisch lan neurofibroma. Scoliosis (kelengkungan balung punggung), gangguan sinau, gangguan penglihatan, cacat mental, sawetara café au lait spots, lan epilepsi uga bisa muncul.

Ora ana perawatan khusus nganti saiki.

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  • Cafe au lait macule katon ing Neurofibromatosis tipe 1 (NF-1)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Akèh neurofibroma cilik.
  • NF-1 — Punggung pasien tuwa.
  • Manifestasi khas NF‑1 yaiku sawetara neurofibroma sing diamati kanthi pigmentasi bintik‑bintik.
  • Pasien sing duwe angiofibroma ing rai disebabake tuberous sclerosis.
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis minangka kondisi sing nyebabake tumor ing sistem saraf lan kulit. Tipe 1 diwarisake sacara dominan lan nuduhake gejala kaya neurofibromas, café‑au‑lait spots, freckling, lan optic gliomas. Diagnosis adhedhasar pratandha klinis. Tipe 2, ing sisih liya, ditandhani kanthi bilateral vestibular schwannomas (VS) lan meningiomas, uga diwarisake sacara dominan. Manajemen kalebu pemantauan rutin lan perawatan medis sing dibutuhake kanggo loro jinis 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.