Ontology highlight
ABSTRACT:
SUBMITTER: Brosseau JP
PROVIDER: S-EPMC7792184 | biostudies-literature | 2021 Jan
REPOSITORIES: biostudies-literature
Acta neuropathologica communications 20210107 1
Neurofibromatosis Type I (NF1) is a neurocutaneous genetic syndrome characterized by a wide spectrum of clinical presentations, including benign peripheral nerve sheath tumor called neurofibroma. These tumors originate from the Schwann cell lineage but other cell types as well as extracellular matrix (ECM) in the neurofibroma microenvironment constitute the majority of the tumor mass. In fact, collagen accounts for up to 50% of the neurofibroma's dry weight. Although the presence of collagens in ...[more]