Neurofibromatosis type 1 is a relatively common genetic disease, with a prevalence ranging
between 1/3000 and 1/6000 people worldwide. The disease affects multiple systems with …

Neurofibromatosis 1 is an autosomal dominant disorder characterized by multiple café-au-
lait spots, axillary and inguinal freckling, multiple cutaneous neurofibromas, and iris Lisch …

Neurofibromatosis 1 (NF1) is a multisystem disorder characterized by multiple café au lait
macules, intertriginous freckling, multiple cutaneous neurofibromas, and learning disability …

Abstract Neurofibromatosis 1 (NF1) is an inherited neurocutaneous disease that has a major
impact on the nervous system, eye, skin, and bone. Individuals with NF1 have a …

Abstract Neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), and
schwannomatosis (SWN) are three clinically distinct tumor predisposition syndromes with a …

Whole-body magnetic resonance (MR) imaging has been evaluated in many oncologic and
rheumatologic indications and is emerging as a powerful tool for early diagnosis …

OBJECTIVE: To characterize morbidity, mortality, and surgical outcomes in pediatric patients
with symptomatic plexiform neurofibromas (PNFs). STUDY DESIGN: We conducted …

Purpose Patients with neurofibromatosis 1 (NF1), NF2, and schwannomatosis are at risk for
multiple nerve sheath tumors and premature mortality. Traditional magnetic resonance …

With advancement in 3D imaging, better fat-suppression techniques, and superior coil
designs for MR imaging and the increasing availability and use of 3T magnets, the …

Neurofibromatosis type 2 (NF2) is a rare autosomal dominant disorder (incidence 1: 33 000-
40 000) characterized by formation of central nervous system tumors, due to mutation in the …