Fig. 2From: LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosisDe-identified images of the patient’s plexiform neurofibromas. Panel A shows cornal T1 sequence, with multiple hypodense lesions arising from the sacral nerve roota, in keeping with neurofibromas (white arrows). Panel B shows sagittal T2 sequence, with neurofibromas seen as hyperintense lesions (white arrows)Back to article page