Neurofibromatosishttps://en.wikipedia.org/wiki/Neurofibromatosis_type_I
Neurofibromatosis multiplex systematis humani inordinationis per mutationem neurofibrominum causata est. Neurofibromatosis tumores facit per nervos, qui alicubi in corpore crescere possunt. Neurofibromatosis una est perturbationes geneticae maxime communes et inordinatio autosomal dominans.

Communes symptomata neurofibromatosis includunt maculas brunneo-ruber in colorata parte oculi, noduli Lisch et neurofibromas vocati. Scoliosis (curvatura spinae), defectus discendi, perturbationes visionis, defectus mentis, multiplices cafe au lait maculae et comitiales etiam comitari possunt.

Nulla certa curatione adhuc.

☆ In anno 2022 Stiftung Warentest ex Germania provenit, satisfactio consumptoria cum ModelDerm paulo minus fuit quam cum consultationibus telemedicinis solutis.
  • Cafe au lait macule videri in Neurofibromatosis type 1 (NF-1)
  • Multiple Neurofibromas (Von Recklinghausen disease)
  • Neurofibroma
  • Multas parvas neurofibromas.
  • nf-1 Senex aegri dorsum.
  • Typicam manifestationem NF-I. Plures neurofibromas pigmentationis punctatae observantur.
  • Patiens cum facie ex causa angiofibroma tuberous sclerosis
References Neurofibromatosis 29083784 
NIH
Neurofibromatosis conditio est quae tumores in systemate nervoso et cute creat. Typus 1 hereditatur dominans et ostendit symptomata sicut neurofibromas, café-au-lait spots, freckling, and optic gliomas. Diagnosis in signis clinicis fundatur. Typus 2, ex altera parte, bilateral vestibular schwannomas (VS) and meningiomas signatur, etiam dominante hereditario. Procuratio regularis vigilantia et curationis medicinae in utraque specie ad neurofibromatosis necessaria est.
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.