Search Results 1-10 of 16547 for Neurofibromatosis+type+1
Neurofibromatosis type 1 (NF1) is a genetic condition that causes changes in skin pigment and tumors on nerve tissue. Skin changes include flat, light brown ...
Diagnosis. To diagnose neurofibromatosis type 1 (NF1), a healthcare professional begins with a review of your personal and family medical history and a ...
Mayo Clinic specialists also have experience with treatment for serious NF1, including surgery. The Neurofibromatosis Clinic also has genetic counselors who can ...
The purpose of this study is to evaluate children ≥ 1 year of age and adults with neurofibromatosis type 1 (NF1) and plexiform neurofibromas treated with the ...
Research. Mayo Clinic researchers study genetics, causes and new treatments for people with neurofibromatosis type 1. Research is conducted by Mayo Clinic ...
The objective of this study is to collect blood samples from living patients with neurofibromatosis type 1 (NF1) for future genomic, proteomic, metabolomic, and ...
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 most ...
At Mayo Clinic, multidisciplinary teams of specialists collaborate to manage neurofibromatosis types 1 and 2 (NF1 and NF2) in children and adults.
Developing Criteria for Treatment of Neurofibromatosis Type 1 Associated Optic Pathway Glioma · Overview · Participation eligibility · Participating Mayo Clinic ...
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