OverviewFrontotemporal dementia
Frontotemporal dementia is an uncommon type of dementia that mainly affects the front and sides of the brain (frontal and temporal lobes) and causes problems with behaviour and language.
Dementia is the name for problems with mental abilities caused by gradual changes and damage in the brain.
Dementia mostly affects people over 65, but frontotemporal dementia tends to start at a younger age. Most cases are diagnosed in people aged 45-65, although it can also affect younger or older people.
Symptoms of frontotemporal dementia
Signs of frontotemporal dementia can include:
- personality and behaviour changes – acting inappropriately or impulsively, appearing selfish or unsympathetic, neglecting personal hygiene, overeating, or loss of motivation
- language problems – speaking slowly, struggling to make the right sounds when saying a word, getting words in the wrong order, or using words incorrectly
- problems with mental abilities – getting distracted easily, struggling with planning and organisation
- memory problems – these only tend to occur later on, unlike more common forms of dementia, such as Alzheimer's disease
There may also be physical problems, such as slow or stiff movements, loss of bladder or bowel control (usually not until later on), muscle weakness or difficulty swallowing.
These problems can make daily activities increasingly difficult, and the person may eventually be unable to look after themselves.
Read more about the symptoms of frontotemporal dementia.
Getting medical advice
See your GP if you think you have early symptoms of dementia. If you're worried about someone else, encourage them to make an appointment with their GP and perhaps suggest you go with them.
Your GP can do some simple checks to try to find the cause of your symptoms, and they can refer you to a memory clinic or another specialist for further tests if needed.
Read more about getting a dementia diagnosis.
Tests for frontotemporal dementia
There's no single test for frontotemporal dementia.
The following may be needed to make a diagnosis:
- an assessment of symptoms – it's normally helpful to have somebody who knows the person well to give an account of their symptoms, especially as someone with frontotemporal dementia may not be aware of changes in their behaviour
- an assessment of mental abilities – this will usually involve a number of tasks and questions
- blood tests – to rule out conditions with similar symptoms
- brain scans – such as an MRI scan, a CT scan or a PET scan; these can detect signs of dementia and help identify which parts of the brain are most affected, or help rule out other problems with the brain
- lumbar puncture – to test the spinal fluid; this may be useful to rule out Alzheimer's disease as the cause of symptoms
Read more about the tests used to diagnose dementia.
Treatments for frontotemporal dementia
There's currently no cure for frontotemporal dementia or any treatment that will slow it down.
But there are treatments that can help control some of the symptoms, possibly for several years.
Treatments include:
- medicines – to control some of the behavioural problems
- therapies – such as physiotherapy, occupational therapy, and speech and language therapy for problems with movement, everyday tasks and communication
- dementia activities – such as memory cafés, which are drop-in sessions for people with memory problems and their carers to get support and advice
- support groups – who can offer tips on managing symptoms from dementia experts and people living with frontotemporal dementia, and their families
Read more about how frontotemporal dementia is treated.
Outlook for frontotemporal dementia
How quickly frontotemporal dementia gets worse varies from person to person and is very difficult to predict.
People with the condition can become socially isolated as the illness progresses. They may not want to spend time in the company of others, or may behave in rude or insulting ways.
Home-based help will usually be needed at some stage, and some people will eventually need care in a nursing home.
The average survival time after symptoms start is around eight years. But this is highly variable and some people live much longer than this.
If you or a loved one has been diagnosed with dementia, remember you're not alone. The NHS and social services, as well as voluntary organisations and specialist support groups, can provide advice and support for you and your family.
Causes of frontotemporal dementia
Frontotemporal dementia is caused by clumps of abnormal protein forming inside brain cells. These are thought to damage the cells and stop them working properly.
The proteins mainly build up in the frontal and temporal lobes of the brain at the front and sides. These are important for controlling language, behaviour, and the ability to plan and organise.
It's not fully understood why this happens, but there's often a genetic link. About one in every three people with frontotemporal dementia has a family history of dementia.
If you have a family history of frontotemporal dementia, you may want to consider talking to your doctor about being referred to a geneticist and possibly having a genetic test to see if you're at risk.
There's a lot of research being done to try to improve understanding of the causes of frontotemporal dementia so treatments can be discovered.
If you're interested in helping with research, you can speak to your doctor or register your interest on Join Dementia Research.
Other names for frontotemporal dementia
Doctors sometimes use different names to describe frontotemporal dementia. These include:
- FTD
- Pick's disease
- frontal dementia
- frontotemporal lobar degeneration
- behavioural variant frontotemporal dementia
- primary progressive aphasia
- semantic dementia
- progressive non-fluent aphasia
More detailed information about these different terms and types of frontotemporal dementia can be found on the FTD Talk website.