Search Results 41-50 of 16656 for Neurofibromatosis
The growths were caused by neurofibromatosis, a condition Sampson was born with. It's a condition that — as we reported when Sampson first came to Rochester ...
The Neurofibromatosis Clinic also has genetic counselors who can help you make decisions that are appropriate for you and your family. Counselors can help ...
She studies and reports new findings in rare genetic disorders and neurocutaneous disorders with focus on neurofibromatosis and schwannomatosis. Dr. Dhamija ...
Multiple endocrine neoplasia, type 1 (MEN 1); Multiple endocrine neoplasia, type 2 (MEN 2); Von Hippel-Lindau disease; Tuberous sclerosis; Neurofibromatosis ...
Neurofibromatosis 2. Tuberous sclerosis. Gorlin syndrome. Turcot syndrome. Cowden syndrome. Tests of your child's DNA can show whether these syndromes are ...
Mayo Clinic's Neurofibromatosis Type 2 Clinic provides expert, multidisciplinary care for teenagers and adults with this tumor-predisposing genetic disorder.
These include neurofibromatosis 1, Noonan syndrome, Li-Fraumeni syndrome, Beckwith-Wiedemann syndrome and Costello syndrome. There is no way to prevent ...
Selumetinib is used to treat neurofibromatosis type 1 (NF1) in children 2 years of age and older who have plexiform neurofibromas that cannot be removed by ...
Pathologically confirmed MPNST, with or without underlying diagnosis of neurofibromatosis type 1 (diagnostic criteria for neurofibromatosis type 1) ...
Title: MEK-NF-201, A Phase 2b Trial of the MEK 1/2 Inhibitor (MEKi) PD-0325901 in Adult and Pediatric Patients With Neurofibromatosis Type 1 (NF1)- ...
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