Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis waa khalkhal kakan oo nidaamyo badan oo biniaadmi ah oo ay sababto isbeddelka neurofibromin. Neurofibromatosis waxay sababtaa burooyin ku teedsan habdhiska neerfaha kuwaas oo ka bixi kara meel kasta oo jidhka ah. Neurofibromatosis waa mid ka mid ah cilladaha hidde-sideyaasha ee ugu caansan iyo cilladda ugu badan ee autosomal.

Calaamadaha caadiga ah ee neurofibromatosis waxaa ka mid ah dhibco guduudan oo casaan ah oo ku yaal qaybta midabka isha ee loo yaqaanno Lisch nodules iyo neurofibromas. Scoliosis (qallooca laf dhabarta), naafonimada waxbarashada, khalkhalka aragga, itaaldarrada maskaxda, maqaaxiyo badan oo kafeega au lait spots iyo suuxdin ayaa sidoo kale la socon kara.

Ilaa hadda ma jirto daaweyn gaar ah.

☆ Natiijooyinka Stiftung Warentest ee 2022 ee ka yimid Jarmalka, ku qanacsanaanta macaamilka ee ModelDerm ayaa waxyar uun ka hooseysay la-talinta telemedicine-ka ee lacagta lagu bixiyo.
  • Cafe au lait macule lagu arkay Neurofibromatosis type 1 (NF-1)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • neurofibromas yar yar oo badan.
  • NF-1 - dhabarka bukaanka waayeelka ah.
  • Muujinta caadiga ah ee NF-1. Tiro neurofibromas ah ayaa lagu arkay midab midab leh.
  • Bukaanka leh wajiga angiofibroma uu sababay tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis waa xaalad keenta burooyin ku dhaca habdhiska neerfaha iyo maqaarka. Nooca 1 aad ayaa loo kala dhaxlaa wuxuuna muujiyaa calaamadaha sida neurofibromas, café-au-lait spots, freckling, and optic gliomas. Cilad-sheegiddu waxay ku salaysan tahay calaamadaha bukaan-socodka. Nooca 2, dhinaca kale, waxaa lagu calaamadeeyay bilateral vestibular schwannomas (VS) and meningiomas , sidoo kale dhaxal ahaan inta badan. Maaraynta waxay ku lug leedahay la socodka joogtada ah iyo daawaynta daawaynta marka loo baahdo labada nooc ee 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.