Neurofibromatosis

In this condition factsheet:

• The Facts
• Causes
• Symptoms and Complications
• Making the Diagnosis
• Treatment and Prevention

The Facts

Neurofibromatosis (NF) is a genetic disorder that affects the nervous system. People affected by this condition develop non-cancerous tumours along their nerves. The tumours are called neurofibromas. They are a mass of different types of cells that grow on and surround nerves.

NF can also cause skin discolourations (also called "café au lait" spots) and bone abnormalities. Men, women, and people of all ethnic backgrounds may develop the condition.

Causes

The cause of NF is a change in a person's genetic material, known as a genetic mutation. There are 2 genes that cause 2 different types of NF: neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2). NF1 was previously known as von Recklinghausen's disease and occurs more commonly than NF2.

NF is a genetic condition. If either parent has the gene for NF, their child will have a 50% chance of inheriting the disease. In about half of the people affected with NF1, the gene mutation occurred spontaneously, meaning that the individual has no family history of the condition. Once the gene changes, NF may be passed on to the next generation.

Symptoms and Complications

The symptoms related to NF1 and NF2 are different.

People with NF1 may have some of the following symptoms:

• noncancerous tumours under the skin (or deeper within the body)
• brown patches in the iris (coloured part of the eye) called Lisch nodules
• bowed legs, short stature, or bone abnormalities including scoliosis (an abnormal side-to-side curve in the spine)
• freckles in the groin or underarm area
• growth of a tumour on the optic nerve (an optic glioma)
• light brown flat skin marks called "café au lait" spots

Because it affects the nervous system, NF1 may cause learning disabilities, speech problems, and delays in an individual's development. Seizures, eye tumours, and high blood pressure may also affect people with this condition. Rarely, the tumours may become malignant (cancerous). In some cases, tumours may also affect organs within the body.

People with NF2 develop tumours that appear on the nerve that connects the ear to the brain. These tumours are also called "schwannomas." Because of their association with the ear, tumours on this nerve may cause hearing difficulties. Other complications related to the ear may include dizziness, ringing in the ears (tinnitus), and balance problems. The pressure from the tumours on other nerves may also cause headaches or numbness of the face or weakened facial muscles.

People who have NF2 may also develop tumours in other body areas, such as the brain and spinal cord. Unlike NF1, skin discolouration and freckles are few or nonexistent in people with NF2.

Cataracts can develop early in life, which may cause vision difficulties or blindness.

Making the Diagnosis

To make the diagnosis, your doctor will do a number of tests and examinations. For NF1, a doctor will discuss your medical history and do a physical examination of your skin to look for "café au lait" spots and freckling. A complete ophthalmologic exam is also recommended. X-rays will help your doctor look for abnormalities in your bone structure.

Doctors usually request tests that confirm tiny tumours on the nerves in both NF1 and NF2. MRI scans may reveal tumours in various parts of the body. Blood tests may also be done to screen for the NF gene. When NF2 is suspected, the doctor may recommend hearing tests to evaluate a person's hearing and the function of the nerve that leads from the ear to the brain.

Treatment and Prevention

No cure exists for NF. Instead, treatment primarily focuses on managing symptoms. In the rare cases of NF1 or NF2 where a tumour becomes cancerous, surgery and radiation may be necessary. This is often complicated as the tumours in NF2 are frequently close to the brain or spinal cord. Also, tumours may recur even after surgical removal. Non-cancerous tumours may be removed if they are causing pain, or for cosmetic reasons.

For children aged 2 to 18 years old with a specific type of NF1 called inoperable plexiform neurofibroma, a medication called selumetinib may be able to decrease the tumour growth.

Medications can help with nerve pain and high blood pressure. There may be related anxiety and depression if present, which should also be treated.

In cases of NF1, surgery can help correct bone deformities. Back braces can be used to provide stability and support for people with scoliosis.

All material copyright MediResource Inc. 1996 – 2025. Terms and conditions of use. The contents herein are for informational purposes only. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Source: www.medbroadcast.com/condition/getcondition/Neurofibromatosis