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

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

Ora ana perawatan khusus nganti saiki.

☆ Ing asil Stiftung Warentest 2022 saka Jerman, kepuasan konsumen karo ModelDerm mung luwih murah tinimbang konsultasi telemedicine sing dibayar.
  • Cafe au lait macule katon ing Neurofibromatosis type 1 (NF-1)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Multiple neurofibroma cilik.
  • NF-1 ― Punggung pasien tuwa.
  • Manifestasi khas NF-1. Sawetara neurofibroma diamati kanthi pigmentasi bintik-bintik.
  • Pasien karo rai angiofibroma 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, and optic gliomas. Diagnosis adhedhasar pratandha klinis. Tipe 2, ing sisih liya, ditandhani kanthi bilateral vestibular schwannomas (VS) and 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.