Search Results 1-10 of 16684 for Neurofibromatosis
Neurofibromatosis type 1 (NF1) is a genetic condition that causes changes in skin pigment and tumors on nerve tissue. Skin changes include flat, ...
To diagnose neurofibromatosis type 1 (NF1), a healthcare professional begins with a review of your personal and family medical history and a physical exam. Your ...
Neurofibromatosis type 2 (NF2) is an uncommon genetic condition that results in the development of multiple brain tumors and spinal tumors.
Mayo Clinic specialists also have experience with treatment for serious NF1, including surgery. The Neurofibromatosis Clinic also has genetic counselors who can ...
Diagnosis. A neurofibroma can arise with no known cause, or it may appear in people with a genetic condition called neurofibromatosis type 1. These tumors are ...
The Neurofibromatosis Clinic brings together specialists with experience managing both NF1 and NF2. Those specialists include: Neuro-oncologists; Neurologic ...
The objective of this study is to collect blood samples from living patients with neurofibromatosis type 1 (NF1) for future genomic, proteomic, metabolomic, and ...
Research. Mayo Clinic researchers study genetics, causes and new treatments for people with neurofibromatosis type 1. Research is conducted by Mayo Clinic ...
We provide clinical evaluations for neurofibromatosis (type 1 and type 2) and schwannomatosis — and all of our physicians have significant experience treating ...
Experts in Mayo's Neurofibromatosis (NF) Clinic evaluate and treat patients who have neurofibromatosis, type 1 and type 2, and schwannomatosis.
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