pharmasites logo
We use cookies to enhance your browsing experience. By clicking 'I Understand and Accept', you consent to our use of cookies.
I understand and accept
No, I don't want to use cookies
My Account
Control Panel
An example toast message
Do Something
Login
en
en
Pharmasites logo.
Menu
en
en
Change Language
Login
My Account
Control Panel
Free Upgrade
What You Get
Pricing
About Us
Contact Us
Book a Chat
Log Out
Login
Login
en
en
Do Something
Login
en
en
Pharmasites logo.
Menu
en
en
Change Language
Login
My Account
Control Panel
Free Upgrade
What You Get
Pricing
About Us
Contact Us
Book a Chat
Log Out
Login
Login
en
en
Neurofibromatosis type 1
Neurofibromatosis type 1

Neurofibromatosis type 1 (NF1) is a genetic condition that causes tumours to grow along your nerves. The tumours are usually non-cancerous (benign) but may cause a range of symptoms.

Neurofibromatosis type 2 (NF2) is much less common than NF1. It's covered separately as it has different symptoms and causes.

Symptoms of neurofibromatosis type 1

NF1 is a condition you're born with, although some symptoms develop gradually over many years. The severity of the condition can vary considerably from person to person.

In most cases, the skin is affected, causing symptoms such as:

  • birthmarks known as café au lait spots, which are light or dark brown patches that can be anywhere on the body
  • soft, non-cancerous tumours on or under the skin (neurofibromas)
  • clusters of freckles in unusual places – such as the armpits, groin and under the breast
  • problems with the bones, eyes and nervous system

Certain health problems are often associated with NF1, such as learning difficulties. Less commonly, NF1 is associated with a type of cancer known as malignant peripheral nerve sheath tumours.

Read more about the symptoms of neurofibromatosis type 1

Causes of neurofibromatosis type 1

NF1 is caused by a faulty gene. If the NF1 gene is faulty, it leads to uncontrolled growth (tumours) developing in the nervous system.

In half of all cases of NF1, the faulty gene is passed from a parent to their child. Only one parent needs to have the faulty gene for their child to be at risk of developing the condition.

If either the mother or father has the faulty gene, there's a 1 in 2 chance that each child they have will develop NF1.

In other cases, the faulty gene appears to develop spontaneously (where there is no family history of NF1). It's unclear why this happens. If you have a child who develops NF1 spontaneously, it's highly unlikely any further children you have will also develop the condition.

However, if you do have a child who develops NF1 spontaneously, they could pass on the condition to any children that they have.

Diagnosing neurofibromatosis type 1

It's usually easy to diagnose NF1 in adults and older children by checking for the typical symptoms.

It may be diagnosed in babies who show symptoms of NF1 from birth. However, it's not always possible to make a firm diagnosis in early childhood because some symptoms take years to develop.

If NF1 is suspected, further tests such as scans, blood tests or a biopsy may be recommended. This is to assess whether your child has other symptoms or conditions associated with NF1.

If there's uncertainty about the diagnosis, your child may be able to have a blood test to see whether they have the faulty NF1 gene. However, the test is not completely reliable: around 5% of children who test negative for the faulty gene still develop NF1.

Before and during pregnancy

Couples with a family history of NF1 may wish to consider their options before having a baby. A GP can refer you to a genetic counsellor to discuss your options.

These may include:

  • having a child with a donor egg or sperm
  • adopting a child
  • having a test during pregnancy – either chorionic villus sampling or amniocentesis to see if your baby will have NF1
  • pre-implantation genetic diagnosis – where eggs are fertilised in a laboratory and tested to make sure they do not have the NF1 gene, before being implanted into the womb
Treatment for neurofibromatosis type 1

There's currently no cure for NF1. Treatment involves regular monitoring and treating any problems as they occur.

Treatment can involve:

  • surgery – to remove tumours and treat problems with bones
  • medicine – to control secondary conditions, such as high blood pressure
  • physiotherapy
  • psychological support
  • pain management

Careful monitoring and treatment can help people with NF1 live a full life. However, there's a risk of developing serious problems, such as certain types of cancer, that can reduce life expectancy.

Read more about treating neurofibromatosis type 1

NF1 and pregnancy

If you become pregnant while living with NF1, you should be able to have a healthy pregnancy.

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.

Support from charities

Nerve Tumours UK is a charity that aims to improve the lives of people with either type of neurofibromatosis.

You can find out more on the Nerve Tumours UK website, call its helpline on 07939 046 030 or email info@nervetumours.org.uk.

The Childhood Tumour Trust also provides information and support for young people and their families who may be affected by NF1.

NF1 and breast cancer

Women under 50 with NF1 have an increased risk of breast cancer and should start having breast screening appointments when they're 40 years old.

Information about you

If you or your child has NF1, your clinical team will pass information on to the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).

This helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.

Find out more about the NCARDRS

Last Reviewed
18 November 2021
NHS websiteNHS website
Pharmasites footer logo.
Store Hours Unavailable
No store selected for opening hours
Loading Open Hours...
With over a decade's experience working with UK pharmacies and supplying software that manages over 1,500 UK pharmacy websites, you're in safe hands with Pharmasites. Get in touch today!
Menu
Home
Free Upgrade
Pricing
Referrer Rewards
About Us
Contact Us
Book a Chat
Features
Easy Website Updates
Interactive Maps
Book NHS & Private Services
Pharmacy First
eCommerce
Built-in NHS A-Z
NHS App Integration
See more features
Pharmasites
11 Anderson Way, Lea, Gainsborough, Lincolnshire, DN21 5EF
matt@pharmasites.co.uk
01904 349 316
No store selected for contacts
No contacts at this store
Pharmasites © 2024
Cookies Policy
Privacy Policy
Terms and Conditions