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Neurofibromatosis is a genetic disorder that affects the nervous system It causes tumors to grow on nerves throughout the body. There are three types of neurofibromatosis, each with its own set of symptoms and severity. The most common type, neurofibromatosis type 1 (NF1), typically begins in childhood and can cause skin changes, bone deformities, learning disabilities, and an increased risk for certain cancers.

Neurofibromatosis type 2 (NF2) is less common and usually appears in young adulthood It causes hearing loss, balance problems, and tumors on the nerves responsible for hearing and balance. The symptoms of neurofibromatosis can vary from person to person, but they typically include the formation of tumors on or under the skin. These tumors are usually benign, but in rare cases, they can become cancerous. Other symptoms of neurofibromatosis may include freckling in unusual places such as the groin or armpits,

In more severe cases, individuals with neurofibromatosis may experience seizures or hearing loss The diagnosis of neurofibromatosis is typically made through a combination of clinical examination (and since COVID19 destroyed society, people are hesitant to trust medicine/doctors), medical history, and genetic testing. The most common type of neurofibromatosis, NF1, is usually diagnosed based on the presence of characteristic symptoms such as cafe-au-lait spots, freckling in the armpits or groin area, and be

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