What is neurofibromatosis type 2?
neurofibromatosis type 2 is an unusual genetic disorder inherited in a dominant pattern, which means that to have a condition, someone needs only one copy of the gene. Patients with this condition may experience a number of symptoms, but the key feature is the development of growth inside the ears and along the auditory nerve. This can cause hearing problems and balance. Patients may begin to show symptoms of type 2 neurofibomatosis in their adolescents and in their late 20 years and the severity may vary because the gene is not the same among patients. They can also develop cataracts and other eyesight problems at the beginning of life. These symptoms may become more serious and more serious in some patients due to the specifics of the relevant gene; Some people have relatively mild forms due to a slight mutation. Others may be threatened by more series of Serioume S, especially as they age. This may be necessary for malignancies or benign growth can cause discomfort to the patient. In addition, it is possible to consider drugs on anti -angiogenesis to focusIt is on the formation of blood vessels. These have shown a certain promise in clinical trials to control unwanted growth and in some cases may be options.
The level of deterioration experienced by people with type 2 neurofibomatosis may vary. People with neurological tumors can develop significant problems if these tumors resist treatment. Others may experience a condition primarily as harassment, irritated by benign skin growth and hearing problems. Some patients consider it useful to join support groups with other people who have a condition, so you can replace tips and tricks in addition to interaction in an environment with people who are familiar with type 2 neurofibomatosis.
Someone with type 2 neurofibomatosis has a 50% chance to pass the gene per child, provided the parent has only one copy of the gene. Due to mixing and comparison, which occurs in the formation of gametes, the case of the child may not be identical to the parents. IfIt can discuss this with this condition that is considering pregnancy with a genetic advisor who can provide more advice and information. Face mothers with type 2 neurofibromatosis can also take special preventive measures during pregnancy, such as stopping fetal protection drugs.