Neurofibromatosis type 1 - Symptoms and causes - Mayo Clinic
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 spots and freckles in the armpits and groin.
Neurofibromatosis type 1 - Diagnosis and treatment - Mayo Clinic
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 child's skin is checked for cafe au lait spots, which can help diagnose NF1.
Neurofibromatosis Type 2 Clinic - Overview - Mayo Clinic
4 天之前 · Neurofibromatosis type 2 (NF2) is an uncommon genetic condition that results in the development of multiple brain tumors and spinal tumors. Almost all people with NF2 have two tumors affecting each of the hearing nerves, called vestibular schwannomas.
Neurofibromatosis tipo 1 - Síntomas y causas - Mayo Clinic
La neurofibromatosis tipo 1 (NF1) es una afección genética que causa cambios en la pigmentación de la piel y tumores en el tejido nervioso. Los cambios en la piel incluyen manchas sin relieve de color marrón claro y pecas en las axilas y en la ingle.
Neurofibromatosis Clinic - Mayo Clinic
2016年4月8日 · Experts in Mayo's Neurofibromatosis (NF) Clinic evaluate and treat patients who have neurofibromatosis, type 1 and type 2, and schwannomatosis.
Neurofibromatosis type 1 care at Mayo Clinic
Mayo Clinic's world-renowned Neurofibromatosis Clinic provides coordinated care for people with this complex condition. Geneticists, adult and pediatric neurologists, neuro-oncologists, radiologists, and neurosurgeons work together to provide exactly the care you need.
Neurofibroma - Diagnosis and treatment - Mayo Clinic
2024年10月5日 · Selumetinib (Koselugo) has been approved to treat a plexiform neurofibroma in children with neurofibromatosis type 1. A plexiform neurofibroma grows on many nerves. The medicine can shrink the tumor. Surgery to remove the tumor. Symptoms can be relieved by removing all or part of a neurofibroma that's pressing on nearby tissue or damaging organs.
Neurofibroma - Symptoms and causes - Mayo Clinic
2024年10月5日 · A neurofibroma can arise with no known cause, or it may appear in people with a genetic condition called neurofibromatosis type 1. Neurofibromas most often are found in people ages 20 to 30 years old.
Neurofibromatosis Clinic - Overview - Mayo Clinic
2024年6月12日 · We provide clinical evaluations for neurofibromatosis (type 1 and type 2) and schwannomatosis — and all of our physicians have significant experience treating patients with these rare and complex conditions.
Schwannomatosis - Symptoms and causes - Mayo Clinic
2024年7月19日 · NF2-related schwannomatosis was previously known as neurofibromatosis 2 (NF2). The other two types of schwannomatosis are SMARCB1-related schwannomatosis and LZTR1-related schwannomatosis. The altered genes that cause these types usually are not passed down through families.