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.

There isn't a cure for neurofibromatosis type 1 (NF1), but symptoms can be managed. Generally, the sooner someone is under the care of a specialist trained in treating NF1, the better the outcome.

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 …

Para diagnosticar la neurofibromatosis tipo 1, deben presentarse, al menos, dos síntomas de la afección. Es probable que se vigile a los niños que solo presentan un síntoma y que no tienen …

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 …

Oct 5, 2024 · Selumetinib (Koselugo) has been approved to treat a plexiform neurofibroma in children with neurofibromatosis type 1. A plexiform neurofibroma grows on many nerves.

Jan 30, 2026 · NF2-related schwannomatosis, previously called neurofibromatosis type 2 or NF2, causes symptoms that usually result from slow-growing tumors in both ears. These tumors are …

Jan 30, 2026 · Regular visits at a center experienced in neurofibromatosis allow early detection of changes and help maintain quality of life. Other targeted medicines and combination approaches are …

Jan 17, 2026 · Learn how a multispecialty team of neurofibromatosis type 2 (NF2) experts can help you understand this lifelong condition and the latest treatment options.

Oct 5, 2024 · The only known risk factor for neurofibromas is having the genetic condition known as neurofibromatosis type 1 (NF1). People with NF1 have several neurofibromas, along with other …