Neurofibromatosis type I with lung involvement in a cancer patient.

@article{Casal2018NeurofibromatosisTI,
  title={Neurofibromatosis type I with lung involvement in a cancer patient.},
  author={Ana Casal and Nuria Rodr{\'i}guez-N{\'u}{\~n}ez and A Mart{\'i}nez-Alegr{\'i}a and Sonia Candamio and J. Victor Alvarez and Luis G Vald{\'e}s},
  journal={Pulmonology},
  year={2018},
  volume={24 4},
  pages={
          269-271
        }
}
Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic syndrome caused by mutations in the NF1 gene that encodes neurofibromin protein which acts as a tumor suppressor. It has a wide range of clinical features, it is characterized by cutaneous signs, notably neurofibromas, café-au-lait macules, iris hamartomas as well as axillary and inguinal… CONTINUE READING