Neurofibromatosis

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    Related websites

    Neurofibromatosis type 1 - Symptoms and causes - Mayo Clinic

    WEBneurofibromatosis 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.

    Mayoclinic.org


    Neurofibromatosis type 1 - Diagnosis and treatment - Mayo Clinic

    WEBTo 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.

    Mayoclinic.org


    Neurofibroma - Overview - Mayo Clinic

    WEBJul 19, 2024 · 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 often found in people ages 20 to 40 years. Your health care provider will look at several factors to diagnose a neurofibroma.

    Mayoclinic.org


    Neurofibromatosis type 1 care at Mayo Clinic

    WEBMayo Clinic specialists use the full array of genetic, imaging, vision and hearing tests to diagnose neurofibromatosis type 1 (NF1). Mayo Clinic specialists also have experience with treatment for serious NF1, including surgery.

    Mayoclinic.org


    Neurofibromatosis Type 2 Clinic - Overview - Mayo Clinic

    WEBJul 9, 2024 · 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.

    Mayoclinic.org


    Neurofibromatosis tipo 1 - Síntomas y causas - Mayo Clinic

    WEBLa 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.

    Mayoclinic.org


    Acoustic neuroma - Symptoms and causes - Mayo Clinic

    WEBJun 20, 2023 · This gene change is inherited in people with a rare disorder called neurofibromatosis type 2. People with neurofibromatosis type 2 usually have growth of tumors on the hearing and balance nerves on both sides of the head. These tumors are known as bilateral vestibular schwannomas.

    Mayoclinic.org


    Neurofibromatosis Clinic - Overview - Mayo Clinic

    WEBJun 12, 2024 · 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.

    Mayoclinic.org


    Schwannomatosis - Symptoms and causes - Mayo Clinic

    WEBJul 19, 2024 · In NF2-related schwannomatosis (NF2), tumors grow in both ears and can cause hearing loss. The altered gene that causes this type is sometimes passed down from a parent. NF2-related schwannomatosis was previously known as neurofibromatosis 2 …

    Mayoclinic.org


    Fibromyalgia - Symptoms & causes - Mayo Clinic

    WEBOct 26, 2021 · Fibromyalgia is a disorder characterized by widespread musculoskeletal pain accompanied by fatigue, sleep, memory and mood issues. Researchers believe that fibromyalgia amplifies painful sensations by affecting the way your brain and spinal cord process painful and nonpainful signals.

    Mayoclinic.org


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