It was his wish that his life and death would somehow help to rekindle the debate in this country and in so doing provide those who have the same wish with the opportunity of fulfilling it when the time comes.
Part Two
1What is Neurofribromatosis?
The following information is published with the kind permission of the Neurofibromatosis Foundation Association, UK.
NEUROFIBROMATOSIS (NF) is a collective name for a group of genetic conditions that affect the nervous system. NF causes benign (non-cancerous) lumps to grow on nerves. These lumps can grow on nerve endings in the skin where they can be seen clearly; the lumps can also grow on deeper nerves within the body.
Neurofibromatosis occurs all over the world in all races. It affects men and women equally.
There are two main types of Neurofibromatosis: Neurofibromatosis type 1 (NF1) and Neurofibromatosis type 2 (NF2).
They are two completely different and separate conditions. People who have NF will have one type or the other. NF1 cannot change into NF2.
NF1 is a common genetic condition. A genetic condition is one that can be passed on in families. Approximately 1 in every 2 500/3 000 people is born with NF1. Many people with NF1 will be affected very mildly and may have nothing more than skin changes.
A minority of people (about a third) who have NF1 will have health problems linked to the diagnosis at some time in their life. Some of these problems will be mild and easily treated, while others will be more severe.
At present, doctors cannot predict who is going to develop health problems linked to having a diagnosis of NF1. Research is helping to identify some individuals at greater risk of developing health complications. Until this is clearer, it is helpful for people to learn more about NF1 to understand what this diagnosis means and to know when to seek medical help.
How is NF1 diagnosed?
The way a doctor can tell if a person has NF1 is by examining them for signs of this condition. There are specific features that the doctor will look for. Signs of NF1 usually appear in childhood (mostly in the first three years of life and almost always before the age of five). The diagnosis of NF1 is confirmed if two or more of the following signs are present:
Six or more flat, café au lait patches (brown coffee-coloured skin patches like a birthmark), which are the size of a pencil top or bigger. These usually appear during the first year of life and can increase in size and number. Café au lait patches are generally harmless and there is no connection between the number or size of café au lait patches and the severity of the condition. They sometimes fade later in life.
Freckles in the armpit or in the groin. Again, these are harmless but can be another sign of NF1.
Neurofibromas (small benign pea-sized growths or lumps) on or under the skin. These are a common feature of NF1. They usually appear during adolescence and tend to increase in number throughout life. Sometimes neurofibromas are present in childhood.
Plexiform neurofibromas. These are a particular kind of neurofibroma. In a plexiform neurofibroma a whole section of the nerve or a group of nerves in one area of the body are affected. Sometimes the overlying skin has a large area of café au lait pigmentation. In adults this can become a red-purple colour. The overlying skin can be more hairy.
Lisch nodules – these are small pigmented areas in the iris (coloured part) of the eye. They are often not visible except during examination with an eye microscope called a slit lamp. Lisch nodules are harmless and never cause symptoms. When identified they help confirm the diagnosis.
A mother, father or child who has NF1.
Why does a person develop NF1?
About half the people who have NF1 are the first person in the family to be affected. The condition has started with them by chance. Our body is made of thousands of cells. These cells contain sets of instructions in the form of genes. The instructions contain chemical codes that ensure the cell works correctly. A change in a gene means it cannot do its job properly. The change in the gene is called a “mutation”. This happens before birth and there is no known reason why it occurs.
Where there are no signs of NF1 in either parent, it means that the gene change (mutation) has occurred for the first time in that individual (child or adult). This is called a “new mutation”.
The other group of people who have NF1 will have inherited the same condition from a parent who also has NF1.
An experienced doctor can diagnose NF1 by way of a careful physical examination. Sometimes the signs of NF1 take time to appear and therefore it may not be possible to make an immediate diagnosis of NF1.
You (or your child) may be asked to come back to see the doctor on another occasion for a second examination. This can be a frustrating and anxious time for parents (or adults) who are under investigation; however, your doctor will want to be sure that the diagnosis of NF1 is correct.
Sometimes a doctor will offer to test for NF1. The genetic blood test for NF1 is getting better all the time but still does not pick up 100% of gene changes – only around 95%. The blood tests are being used more and more to aid diagnosis, particularly where neither parent is affected.
NF1 does not skip generations. There are two ways in which NF1 occurs: it crops up out of the blue as a first event in an individual or it is inherited from an affected parent.
How does NF1 affect the body and what can be done about this?
If someone has NF1, he or she will have it for life. There is as yet no specific
