Yvette (54) a journalist from Kent, started experiencing pain in her hip seven years ago in 2015. An ex-national gymnast who had been incredibly active and flexible her whole life, Yvette felt concerned about the growing discomfort impacting her quality of life, and so sought help from her GP.
Neurofibromatosis
NF1 AND NF2
Our multi-disciplinary neuroscience team can diagnose neurofibromatosis and treat complications of the condition
About
Neurofibromatosis are genetic disorders where benign growths affect the nervous system. There are two types:
NF1: this is a “mistake” in the gene on chromosome 17. Complications can vary in severity and to the individual.
NF2: these are benign nervous system tumours in the brain and spine, causing hearing loss, deafness and mobility problems.
Need to know
NF1 can cause a wide-range of symptoms and affect the skin, eyes and development. It also affects the brain, causing migraines and a small risk of brain tumours and epilepsy in children. The most characteristic sign of NF1 is coffee-coloured blotches on the skin called 'café au lait' spots. People with NF1 may also develop peripheral nerve tumours. This is where an existing peripheral nerve tumour becomes cancerous. Symptoms of an MPNST include:
- an existing neurofibroma growing larger
- chronic pain
- finding it hard to breathe
- weakness, numbness or tingling in the arms and legs
- urinary and bowel incontinence
Both NF1 and NF2 are diagnosed through physical examinations and tests. Your consultants will discuss your symptoms with you and help to make a diagnosis. They may order a number of tests, including:
- Imaging tests: these can display brain and spinal cord tumours and bone abnormalities.
- Genetic tests: it's possible to identify NF1 and NF2 in the womb. Your consultant will give you further information.
Patient stories
This content is intended for general information only and does not replace the need for personal advice from a qualified health professional.