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- Neurofibromatosis Type 1 (NF1) and Neurofibromatosis Type 2 (NF2) are two distinct genetic conditions1234:
- NF1 is more common and characterized by brownish cafe-au-lait spots on the skin, tumors called neurofibromas, and bone deformities.
- NF2 primarily affects the auditory nerves, leading to hearing loss, and can also cause tumors in other nerves.
- NF1 is caused by a mutation on chromosome 17, while NF2 is caused by a mutation on chromosome 22.
Learn more:✕This summary was generated using AI based on multiple online sources. To view the original source information, use the "Learn more" links.Whereas in NF1, the tumors occur in the small nerves of the skin and the large nerves inside your body, in NF2, tumors primarily affect the auditory nerves that connect the ears to the brain and control hearing. NF2 patients can also develop tumors in the nerves of their body.www.mountsinai.org/care/neurology/services/neuro…Scientists have classified NF into two distinct types: neurofibromatosis type 1 (NF1) and NF2. NF1, formerly known as von Recklinghausen's NF, is the more common of the types. It occurs in approximately 1 in 4,000 births. NF2, also referred to as bilateral acoustic NF, central NF or vestibular NF, occurs less frequently- 1 in 40,000 births.www.genome.gov/Genetic-Disorders/Neurofibroma…Both NF1 and NF2 are genetic conditions that affect nerve tissue, but NF1 and NF2 have different symptoms. NF1, far more common than NF2, is characterized by brownish cafe-au-lait spots on the skin and tumors called neurofibromas. NF1 can also cause deformity of bones and has several other manifestations.www.hopkinsmedicine.org/health/conditions-and-di…NF1 and NF2 occur as a result of defects in different genes. NF1 is caused by a mutation on the neurofibromin gene located on the pericentromeric region of chromosome 17. NF2 is caused by a mutation on chromosome 22.dermnetnz.org/topics/neurofibromatosis Neurofibromatosis 1 and 2: Symptoms, Treatments, …
WEBApr 26, 2022 — Neurofibromatosis is a genetic disorder of the nervous system that causes tumors to form on nerve tissues. Learn about the …
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WEBLearn about the two types of neurofibromatosis, a genetic disorder that causes skin and brain tumors. NF1 is characterized by café-au-lait spots and neurofibromas, while NF2 affects the eighth cranial nerve and hearing.
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WEBNeurofibromatosis is a genetic disorder that causes tumors to form along the peripheral nerves. It has three types: NF1, NF2 and schwannomatosis, each with different symptoms and complications. Learn more about the …
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WEBNeurofibromatosis type 1 (NF1) is a genetic disorder that can cause brain tumors, skin tumors, bone deformities and other complications. Learn about the diagnosis, genetic testing and treatment options for NF1 at Johns …
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WEBOct 3, 2022 — Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder characterized by the development of multiple tumors involving the central nervous system (CNS). Bilateral vestibular schwannomas are …
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