Is Neurofibromatosis a terminal?
Is Neurofibromatosis a terminal?
Neurofibromatosis Type 1 (NF1) In most cases, symptoms of NF1 are relatively mild, allowing patients to live normal and productive lives. However, the disorder can also be debilitating and, in some cases, life-threatening.
How is neurofibromatosis 2 inherited?
Neurofibromatosis type 2 is considered to have an autosomal dominant pattern of inheritance. People with this condition are born with one mutated copy of the NF2 gene in each cell. In about half of cases, the altered gene is inherited from an affected parent .
Is neurofibromatosis type 2 curable?
While there is currently no cure for NF2, there are clinical trials available at the Johns Hopkins Comprehensive Neurofibromatosis (NF) Center.
What does neurofibromatosis type 2 mean in medical dictionary?
Neurofibromatosis type 2: A genetic disorder that is characterized by the growth of benign tumors of both acoustic nerves (the nerves to the ears). These tumors, called acoustic neuromas, cause tinnitus (ringing in the ears), hearing loss, and problems with balance. Abbreviated NF2.
What does Neurofibromatosis 2 mean?
Neurofibromatosis type 2 is a disorder characterized by the growth of noncancerous tumors in the nervous system. The most common tumors associated with neurofibromatosis type 2 are called vestibular schwannomas or acoustic neuromas.
How do people get NF1?
Although many people with NF1 inherit the gene that causes the condition, between 30 and 50 percent of cases arise from a spontaneous genetic mutation in the NF1 gene. Once this mutation has occurred, the abnormal gene can be inherited. Each child of an affected parent has a 50 percent chance of inheriting the gene mutation.
What is neurofibromatosis caused by?
Neurofibromatosis is caused by genetic mutations which is either inherited or occur on its own during conception. The gene mutation involved decides which form of Neurofibromatosis the child will have.
