What is neurofibromatosis type 1?
Neurofibromatosis type 1 is a inherited condition where people experience skin changes and benign tumors throughout the body. It monitors the dominant pattern of inheritance and children of people with this condition have 50% chance of its development itself, because they only need to inherit one copy of the defective 17. The chromosome involved. This condition is not curable, but treatment is available for managing symptoms and causing patients to feel more comfortable. People may also know this genetic disorder on behalf of "von Reglinghausen Claly", referring to the first researcher to document and describe it. These increases in number with age. In cases where someone does not have a family history of this disease, but has more than five such places, the doctor may suspect type 1 neurofibomatosis and could recommend diagnostic testing. Nodes can also occur inside the iris of the eye, even if they do not disrupt the patient's vision.
While these tumors will not spread to other areas of the body, they can cause damage. They can damage nerves, put pressure on the surrounding structures or deform bones. Patients with type 1 neurofibromatosis have an increased risk of scoliosis. It is also more likely to experience cancer such as leukemia, and can exert high blood pressure. The severity and accurate combination of symptoms may vary. In patients who experience this as a spontaneous genetic mutation, neither parent will have the disease.
Treatment focuses on solving symptoms. Surgery is available to treat tumors and patients can wear braces for scoliosis. The patient may also undergo routine screening to catch cancer and other hairs, saying that they will be used in time and some lifestyle adjustments to deal with apparent risk factors for things such as high blood pressure to reduce the chances of developing secondary complications. A patient with type 1 neurofibomatosis may need aidsKY for mobility and other assistance devices, depending on how serious the disease and how it affects the patient's body.
people with this disease usually do not have fertility problems as a result, even if they may have unrelated fertility problems. Usually there are no reasons why they cannot have children. A genetic advisor can offer advice and help with reproduction decisions, as parents may be concerned about the transmission of genetic diseases to their children and future generations.