Nf1 Research Paper

There is a 50% chance of being born with neurofibromatosis, if a parent has acquired it in his or her lifetime. There are two types of neurofibromatosis, type 1, and type 2. Neurofibromatosis is a genetic disorder that causes tumors to form on nerve tissue. Most people don’t hear about it, because it’s not a well known disease. Despite the fact that it is a little known disease neurofibromatosis is pervasive and often debilitating. NF is a little known neurological disease that has many identities. The disease may be known by many different names: neurofibromatosis 1 or NF1, Peripheral neurofibromatosis, Recklinghausen Nerve Disease, Von Recklinghausen Disease ( Neurofibromatosis type 1). Because it is known by so many different names its symptoms and hallmarks are often identified with other diseases. Because there are other diseases it makes it hard for doctors to NF presents itself in two main ways. The first and most common presentation is NF1. A diagnosis of NF1 happens one of two ways. The disease can be diagnosed at birth with the presentation of cafe au lait spots which are spots on the skin that
These tumors are called meningiomas. They are slow-growing tumors which usually present on the surface of the brain. Symptoms may occur if they are pressing along the spinal cord or brain. Meningiomas can cause seizures. The seizures can be relatively small such as twitching, jerks, and spasms. They can also be more intense such as a Grand Mal seizure which can include loss of consciousness and body tone and loss of control of bodily functions. Patients may endure sensory loss, and severe headaches, and personality or memory changes ( Cancer.net ). Because NF2 can have such serious manifestations, it is considered more serious than NF1. However, both versions of the disease can have a serious impact on an individual’s