Nörofibromatoz ve kanser Çağrılı Editör

  title={N{\"o}rofibromatoz ve kanser Çağrılı Edit{\"o}r},
  author={Rejin Kebudi},
Neurofibromatosis type 1 NF1 is one of the most common genetic disorders and the major constituent of a family of diseases with widespread manifestations including skin viscera nervous system and eyes clinically known as “phakomatoses” Patients with NF1 carry a high risk of tumor formation The most common central nervous tumor in NF1 is the optic pathway glioma OPG 0 6 of all childhood malignancies are associated with NF1 In patients with NF1 while the risk of developing OPG is 1000 times more… CONTINUE READING