For many people with neurofibromatosis type 1 (NF1), the condition is mild and causes no serious health problems. But some people will have severe symptoms.
NF1 can affect several areas of the body, but it's unlikely someone with the condition will develop all the symptoms below.
The most common symptom of NF1 is the appearance of painless coffee-coloured patches on the skin, known as café au lait spots. They affect 95% of people with NF1. The spots can be present at birth or develop by the time a child is three years old.
During childhood, most children with NF1 will have at least six café au lait spots around 5mm across. These grow to about 15mm during adulthood.
The number of café au lait spots someone has isn't related to the severity of the condition. For example, a person with 10 spots has the same chance of developing further problems as someone with 100 spots.
Having a couple of café au lait spots doesn't necessarily mean you have NF1. About one in 10 people without the condition have one or two of these spots.
Another common symptom of NF1 is clusters of freckles in unusual places, such as the armpits, groin and under the breast.
As a child gets older, usually during teenage years or early adulthood, they develop bumps on or under their skin (neurofibromas). These are caused by non-cancerous tumours that develop on the coverings of nerves. They may vary in size, from pea-sized to slightly bigger tumours. Some neurofibromas have a purple colour.
The number of neurofibromas a person has can vary. Some people only have a small number while others have them on large sections of their body.
Most neurofibromas aren't particularly painful, but may look unattractive, catch on clothes and occasionally cause irritation and stinging.
However, if neurofibromas develop where multiple branches of nerves come together (plexiform neurofibromas), they can cause large swellings. Plexiform neurofibromas sometimes occur on the skin, but may also develop on larger nerves deeper in the body. They may sometimes cause symptoms including pain, weakness, numbness, bleeding, or bladder or bowel changes.
Some children with NF1 develop learning and behavioural problems. It's unclear why this happens. Around 60% of children with NF1 have a learning difficulty, which is usually mild.
One way of measuring intelligence is using a scoring system known as an intelligence quotient (IQ). Average intelligence is set at an IQ of 100.
Children with NF1 who have a learning difficulty may have normal or slightly lower than average intelligence. Most children with NF1 can be taught at a mainstream school. They may have specific learning problems such as difficulty with reading, writing, maths and co-ordination.
The behavioural condition Attention Deficit Hyperactivity Disorder (ADHD) affects around half of all children with NF1. Children with ADHD have problems with attention span, concentration and controlling impulses. NF1 has also been linked with Autism Spectrum Disorder (ASD) and some children may have difficulty in social communication.
Around 15% of children with NF1 develop a tumour on their optic pathway. The optic pathway is located at the back of each eye and sends information from the eyes to the brain. This type of tumour is known as an optic pathway glioma (OPG).
Children under seven years of age are known to have the highest risk of developing this type of tumour. Many are small, grow slowly and don't cause any noticeable symptoms. Children with faster-growing OPGs may have problems with their vision, including:
Younger children may be unable to explain that they have vision problems. You should be aware of any indications your child has difficulty seeing, such as problems picking up small objects or bumping into things. The best way of detecting these tumours is to have eye tests at least every year until your child is at least seven years old.
Another common feature of NF1 is the appearance of tiny brown spots in the iris (the coloured, central part of the eye). These are known as Lisch nodules and don't usually cause any noticeable symptoms or vision problems.
Some children with NF1 develop high blood pressure. This is thought to be because the normal workings of the kidneys are affected by narrowing of the arteries. The kidneys help keep blood pressure at a healthy level.
In rare cases, high blood pressure may be caused by a tumour called a phaeochromocytoma. This causes a release of certain hormones, such as adrenaline, which raise blood pressure.
High blood pressure may be associated with potentially serious complications, such as a stroke or a heart attack, if it's not treated. Children and adults with NF1 are recommended to have regular blood pressure checks, usually at least once a year.
Many children with NF1 have one or more problems affecting their physical development. These can include:
Around 2% of children with NF1 develop pseudarthrosis. This is when abnormal bone development leads to a minor bone fracture, usually in the bone of the lower leg (the tibia). In rare cases, the condition can affect long bones in the arm (ulnar or radius).
The fracture doesn't heal completely, which affects the normal movement of the leg. This usually causes it to curve, known as leg bowing.
Some people with NF1 have very low levels of vitamin D. Vitamin D is needed to keep the bones strong. Vitamin D comes from sunlight and may be found in milk, cheese, yoghurt and oily fish.
Symptoms affecting the brain and nervous system are relatively common in NF1.
Many people with NF1 experience migraines, although they're not specific to NF1 and are common in people who don't have the condition.
Around 5% of people develop brain tumours. The tumours may cause no noticeable symptoms. However, tumours in certain parts of the brain occasionally cause symptoms, such as:
Around 7% of children with NF1 develop epilepsy, where a person has repeated seizures or fits. This tends to be a mild form of epilepsy that's controlled easily with medication.
One of the most serious problems that can affect a person with NF1 is a malignant peripheral nerve sheath tumour (MPNST).
MPNSTs are a type of cancer that develops within a plexiform neurofibroma (see above). It's estimated that people with NF1 have a 10% chance over their lifetime of developing a MPNST. Most cases first develop when people are in their late twenties or early thirties, but can occur at any age.
Symptoms of an MPNST include:
If you have any of these symptoms, contact the doctor in charge of your care as soon as possible.
You should be referred to a specialist centre with experience in diagnosing and treating MPNST.
There are currently two such centres, one in Guy’s & St Thomas’ NHS Foundation Trust in London and the other in the Central Manchester University Hospitals NHS Foundation Trust.
Most women with NF1 have healthy pregnancies.
However, the number of neurofibromas may increase because of hormone changes. Make sure you're cared for by an obstetrician with knowledge of NF1, or speak to your NF1 specialist.