Although the neurofibromatoses consist of at least three autosomal dominantly inherited
disorders, neurofibromatosis 1 (NF1), neurofibromatosis 2 (NF2), and schwannomatosis …

BACKGROUND Neurofibromatosis type 2 (NF2) is a highly penetrant autosomal dominant
condition predisposing affected individuals to schwannomas and meningiomas. The …

Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary neurocutaneous
syndrome characterized by multi‐system involvement and an increased incidence of both …

Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder with variable expression.
The complications are age specific. Neurologic complications include tumors of the …

The neurofibromatoses are a heterogeneous group of hereditary cancer syndromes that
lead to tumors of the central and peripheral nervous systems, as well as other organ …

Neurofibromatoses are made up of at least three autosomal dominantly inherited disorders,
neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2) and schwannomatosis. For …

Background: To date, few pediatric series of neurofibromatosis type 1 (NF-1) have been
described in the literature even though it is the most frequently encountered phakomatosis …

Neurofibromatosis type 1 (NF1) is a cancer predisposition syndrome with an incidence of 1:
2,000. Patients with NF1 have an increased cancer risk and mortality, but there are no …

Background: Neurofibromatosis type 2 (NF2) is an autosomal dominant disease
characterised by the development of multiple nervous system tumours, ocular abnormalities …

Neurofibromatosis 2 (NF2) is an autosomal-dominant condition that causes multiple benign
nervous system tumors, especially vestibular schwannoma. Although frequently confused …