Multiple granular cell tumors in a child with Noonan syndrome.

@article{Bamps2013MultipleGC,
  title={Multiple granular cell tumors in a child with Noonan syndrome.},
  author={Sven Bamps and Tom Oyen and Eric Legius and Joost Vandenoord and Margueritte Stas},
  journal={European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie},
  year={2013},
  volume={23 3},
  pages={257-9}
}
Noonan syndrome was first described by Jacqueline Noonan and its estimated prevalence is 1:1000 to 1:2500 live births.1,2 It is an autosomal dominant genetic disorder characterized by short stature, distinct facial features (broad forehead, hypertelorism, ptosis of the eyelids, epicanthal folds, and low implanted posteriorly rotated ears), a webbed neck… CONTINUE READING