Neurofibromatosis type II

Neurofibromatosis type II (NF2) is a genetic disorder characterized by the growth of noncancerous tumors in the nervous system. The most common tumors associated with NF2 are vestibular schwannomas, which grow on the nerves responsible for balance and hearing leading to the inner ear.

Symptoms[edit | edit source]

The symptoms of NF2 can vary widely among individuals. The most common symptoms include hearing loss, ringing in the ears (tinnitus), and problems with balance. Other symptoms can include weakness or numbness in the arms or legs, pain, and vision problems.

Causes[edit | edit source]

NF2 is caused by mutations in the NF2 gene, which provides instructions for making a protein called merlin. Merlin acts as a tumor suppressor, which means it regulates cell growth and prevents cells from dividing too rapidly or in an uncontrolled way. Mutations in the NF2 gene lead to the production of an abnormal version of the merlin protein that cannot regulate cell growth and division. As a result, tumors (particularly vestibular schwannomas) develop.

Diagnosis[edit | edit source]

Diagnosis of NF2 is based on clinical criteria. These include the presence of bilateral vestibular schwannomas, or a first-degree relative with NF2 and either a unilateral vestibular schwannoma or two of the following: meningioma, glioma, schwannoma, or juvenile posterior subcapsular lenticular opacity.

Treatment[edit | edit source]

Treatment for NF2 varies depending on the size and location of the tumors and the severity of symptoms. Options include surgery, radiation therapy, and medication. Regular monitoring is necessary to track the growth of tumors and manage symptoms.

Prognosis[edit | edit source]

The prognosis for individuals with NF2 varies. Some people live normal, productive lives, while others may become severely disabled. The severity of the disease can vary even among members of the same family.