Search Results 1-10 of 16341 for Neurofibromatosis type 2
Neurofibromatosis type 2 (NF2) is an uncommon genetic condition that results in the development of multiple brain tumors and spinal tumors.
People with neurofibromatosis type 2 usually have growth of tumors on the hearing and balance nerves on both sides of the head. These tumors are known as ...
Neurofibromatosis type 1 (NF1) is a genetic condition that causes changes in skin pigment and tumors on nerve tissue. Skin changes include flat, ...
Providers in 12 specialties collaborate to provide timely diagnosis and treatment for teenagers and adults with neurofibromatosis 2 (NF2).
The altered gene that causes this type is sometimes passed down from a parent. NF2-related schwannomatosis was previously known as neurofibromatosis 2 (NF2).
Both NF1 and NF2 are characterized by the presence of nerve sheath tumors. Over time, NF1 and NF2 can cause wide ...
People who have NF2-related schwannomatosis (NF2) and have hearing loss, brain stem compression or tumor growth, may need surgery to remove acoustic neuromas.
The purpose of this study is to test multiple experimental therapies simultaneously in patients with neurofibromatosis type 2 (NF2) with associated ...
The objective of this study is to collect blood samples from living patients with neurofibromatosis type 1 (NF1) for future genomic, proteomic, metabolomic, and ...
Mayo Clinic's Neurofibromatosis Type 2 Clinic provides expert, multidisciplinary care for teenagers and adults with this tumor-predisposing genetic disorder.
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