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Types of dementia explained

“Dementia” is an umbrella word. Knowing which type someone has helps you understand what to expect and find the right support.

⏱ 4 min read📑 11 sections📚 19 sources✅ Reviewed October 2026

By the numbers

How common each type is, and how long diagnosis can take.

How common

60–80%of dementia cases are caused by Alzheimer’s disease (Alzheimer’s Association).
1 million+people in the U.S. live with Lewy body dementia, the second most common neurodegenerative dementia.
5–10%of people with dementia have vascular dementia alone. It is more common as part of mixed dementia.
~60,000estimated U.S. cases of frontotemporal degeneration (FTD).

Age

1 in 3people age 85 or older may have some form of dementia. But it is not a normal part of aging.
60%of people with frontotemporal dementia are 45 to 64 years old.
50+Lewy body dementia typically begins at age 50 or older.
~40%of 6,196 people studied after death (average age 88) may have had LATE, a recently described type.

Diagnosis

3.6 yearsis the average time it takes to get an accurate FTD diagnosis. It is often first mistaken for depression, Alzheimer’s or a psychiatric condition.
2–20 yearsis the range for how long Lewy body dementia lasts after diagnosis (5 to 7 years on average). Every person is different.

Why the type matters

Different brain changes, different first signs, different care.

Dementia is the loss of thinking, remembering and reasoning to the point that it gets in the way of daily life. It happens when brain cells stop working, lose connections and die. Different diseases cause this in different ways and in different parts of the brain.

That is why one person’s dementia starts with memory, another’s with personality, and another’s with movement or seeing things that aren’t there. The types can look alike, so a careful diagnosis matters.

Knowing the type can help a person

  • Avoid treatments that could cause harm for their type
  • Build the right care team
  • Find support from others with the same diagnosis
  • Plan ahead for medical, legal and money matters
  • Understand what is happening, which many people find a relief
This guide explains, it doesn’t diagnose. Only a qualified professional can tell what is causing changes in thinking. If you are worried, please talk with your clinical provider.

Alzheimer’s disease

The most common type, which usually starts with new memories.

Alzheimer’s disease causes 60–80% of dementia cases. Its most common early sign is trouble remembering newly learned information, like a recent conversation or where something was put.

🔬 What happens in the brainProtein clumps build up and harm brain cells.
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In Alzheimer’s, abnormal proteins called amyloid and tau build up in the brain. Over time, brain cells lose their connections and die.

📈 How it often unfoldsSlow change over years.
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Changes usually come on gradually. Early on, a person may repeat questions or lose track of dates. Later, language, planning, finding the way and daily care can be affected.

The Dementia: understanding it guide walks through early, middle and late stages.
🧑‍💼 Younger-onset Alzheimer’sWhen it starts before 65.
Read more

Alzheimer’s that affects someone under 65 is called younger-onset. It can come while a person is still working and raising a family.

See “When dementia comes early” in Dementia: understanding it, and Dementia runs in my family for genes.

Vascular dementia

Linked to blood flow, and often to heart health.

Vascular dementia happens when conditions damage blood vessels in the brain or cut off the flow of blood and oxygen. Any condition that harms blood vessels anywhere in the body can cause brain changes linked to it.

⚡ Sudden changesAfter a major stroke.
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Thinking can change suddenly after a stroke that blocks a large blood vessel in the brain.

🐢 Gradual changesFrom small strokes or small vessel disease.
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Mild changes can slowly get worse over time from many minor strokes or disease in the brain’s small blood vessels.

🧭 Planning before memoryEarly signs can look different from Alzheimer’s.
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Trouble with planning and judgment can be an early sign. Memory loss may or may not be a big symptom, depending on which brain areas are affected.

❤️ Heart and brainShared risks.
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Risk factors overlap with heart disease and stroke. Not smoking, staying active, and managing blood pressure, cholesterol and blood sugar with your care team are recommended.

Lewy body dementia

Thinking, movement, sleep and seeing things that aren’t there.

Lewy body dementia (LBD) is caused by clumps of a protein called alpha-synuclein, known as Lewy bodies. They affect brain chemicals, which can change thinking, movement, sleep, behavior, mood and automatic body functions.

🔀 Two related formsWhich symptoms come first.
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In dementia with Lewy bodies, thinking changes come first, and movement changes may come later or not at all. In Parkinson’s disease dementia, a person has Parkinson’s movement symptoms first, and thinking changes appear more than a year later.

Over time, people with either form develop similar symptoms, because the same brain changes cause both.

🌗 Good days and bad daysAlertness can change a lot.
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Attention and alertness can shift from day to day or even hour to hour. A person may stare into space, seem very drowsy, or seem much better one day and worse the next.

Families can keep a simple diary of good and bad times. It helps doctors see the pattern.
🐈 Seeing thingsVisual hallucinations are common, often early.
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Most people with LBD see things that aren’t there, often early on. They are usually detailed and realistic, like children or animals.

What can help

  • Stay calm and reassure, rather than arguing
  • Check lighting and shadows that could be misread
  • Tell the care team, especially if the person is frightened
🛌 Acting out dreamsA sleep change that can come years earlier.
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In REM sleep behavior disorder, people seem to act out their dreams by talking, shouting or moving. It can appear years before other LBD symptoms. Daytime sleepiness is also common.

🚶 Movement and bodyStiffness, falls, dizziness and more.
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Changes can include

  • Balance problems and falls
  • Dizziness on standing
  • Smaller handwriting
  • Softer voice
  • Slowness or stiffness
  • Trouble swallowing

LBD is often misdiagnosed because early symptoms can look like Alzheimer’s or a psychiatric illness. It may take more than one visit. Neurologists who focus on memory or movement often have the most experience.

Frontotemporal disorders (FTD)

Often younger, and often starts with personality, language or movement.

Frontotemporal disorders damage the front and side parts of the brain, which help manage behavior, emotions, language and movement. FTD is the most common form of dementia for people under 60.

🙃 Behavioral variant (bvFTD)The most common type: changes in personality and judgment.
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People may act out of character, seem to lack empathy, or have trouble reading social signals. Often they don’t realize their behavior has changed. Memory may stay fairly good at first.

These changes are caused by illness, not by choice. Families often feel hurt or embarrassed. Learning about FTD can ease blame on all sides.
🗣️ Primary progressive aphasia (PPA)Language changes come first.
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PPA affects the ability to speak, read, write and understand words. In one type, people lose the meaning of words and may stop recognizing familiar faces or objects. In another, speaking gets harder and small linking words like “to” or “the” may drop out. There are three types in all.

What can help

  • Speech-language therapy
  • Picture boards, gestures and writing
  • Giving extra time to answer
🦾 Movement typesCorticobasal syndrome, PSP and FTD with ALS.
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Some frontotemporal disorders mainly affect movement. Corticobasal syndrome makes it hard to use the hands for tasks like buttons. Progressive supranuclear palsy causes balance problems, falls and trouble moving the eyes, especially looking down. Some people have FTD together with ALS.

Because the first signs are often in behavior or mood, FTD is frequently mistaken for depression, Alzheimer’s, Parkinson’s or a psychiatric condition. Progression varies widely, from 2 to over 20 years.

Mixed dementia and LATE

When more than one cause is at work, especially in older age.

Many older people with dementia have more than one kind of brain change at the same time, such as Alzheimer’s changes plus blood vessel damage. This is called mixed dementia. It was found in brain studies of older adults after death.

🧬 LATEA recently described type that looks like Alzheimer’s.
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LATE (limbic-predominant age-related TDP-43 encephalopathy) causes Alzheimer’s-like problems with memory and thinking, but a different protein is involved. It tends to affect people over 80.

Right now LATE cannot be diagnosed in living people. Researchers are working on ways to do this.

🧩 What mixed causes mean for familiesSymptoms may not fit one neat box.
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If symptoms don’t match a single type, that doesn’t mean doctors got it wrong. More than one process may be involved. Good care focuses on the person’s needs, whatever the label.

Treatable look-alikes and rarer causes

Some memory problems can be helped, stopped or even reversed.

Not every memory problem is dementia. Tumors, low vitamin levels, side effects of some treatments, and problems with the thyroid, kidneys or liver can cause serious memory trouble that looks like dementia. Some of these can be stopped or even reversed with treatment.

💧 Normal pressure hydrocephalus (NPH)Walking, bladder and thinking changes.
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NPH is a slow buildup of fluid in the brain. It causes problems with walking (feet can feel “stuck”), bladder control and thinking. It is most common in older adults.

NPH often improves with treatment, and early diagnosis improves the chance of a good recovery.

😔 Depression and other mental health conditionsLow mood can affect focus and memory.
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If mood or behavior has changed, a mental health evaluation may be suggested, to see whether depression or another condition is causing or adding to the symptoms.

📚 Rarer causesOther conditions that can cause dementia.
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Examples

  • Chronic traumatic encephalopathy (CTE), from repeated head injuries
  • Creutzfeldt-Jakob disease, a rare brain disorder
  • HIV-associated dementia, when the virus affects the brain
  • Huntington’s disease, an inherited brain disease

For head injuries, see the Concussion guide.

This is one big reason to get checked early, rather than assuming memory changes are “just dementia” or “just age.”

How doctors tell the types apart

History, exams, tests and scans, sometimes over several visits.

Doctors first look for any treatable condition. Then they piece together which type of dementia fits best. There is rarely one single test.

🗒️ Your storyWhat changed first matters a lot.
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Doctors ask how and when symptoms began, about changes in behavior and personality, and about family history.

The “What changed first” worksheet helps you bring clear notes.
🧪 Exams and lab testsRuling other causes in or out.
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A physical exam and blood or other lab tests check hormones, vitamins and other levels that could explain symptoms. Tests of memory, problem solving, language and math look at thinking skills.

🧲 Brain scansCT, MRI and PET.
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Scans can show strokes, tumors and other problems, and changes in the brain’s structure or activity. Patterns can point toward one type or another.

🔬 Newer testsSpinal fluid and blood tests.
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Measuring proteins in spinal fluid can help diagnose Alzheimer’s or other types. Some doctors can order a blood test for amyloid, but blood test results alone should not be used to diagnose dementia, and availability is still limited.

🧑‍⚕️ Who to seeStart with primary care, then a specialist.
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A primary care provider is often the first step. Neurologists, geriatric psychiatrists, neuropsychologists and geriatricians may help diagnose dementia. If there is no specialist nearby, a medical school neurology department can give a referral.

Some tests may not be covered by insurance. It is okay to ask your care team which tests are needed and what they will cost.

How community helps

Finding people who know your type of dementia.

Rarer types like LBD and FTD can feel lonely, because friends and even some professionals may never have heard of them. Groups focused on one type connect families with people who understand their daily reality.

Ways community can help

  • Caregiver groups for a specific type, in person, by phone or online
  • Explaining the type to friends, so odd behavior isn’t judged
  • Memory cafés and faith or community groups that welcome people with dementia
  • Research studies, for people who want to take part
The “Explaining our diagnosis” worksheet can help you find simple words to share with others.

When and where to get help

Helplines for each type, and crisis support.

Talk with your clinical provider if

  • Changes in memory, behavior, language or movement are getting in the way of daily life
  • Someone sees things that aren’t there, or acts out dreams
  • Symptoms change suddenly
  • You have a diagnosis but symptoms don’t seem to fit it
📞 Alzheimer’s Association 24/7 Helpline1-800-272-3900, day or night, for any type of dementia.
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Free, confidential support for people living with dementia, caregivers and families, at 1-800-272-3900.

👁️ Lewy Line800-539-9767, from the Lewy Body Dementia Association.
Read more

The Lewy Body Dementia Association’s Lewy Line (800-539-9767) offers information and support for people with LBD and their families.

🎭 AFTD HelpLine866-507-7222, for frontotemporal disorders.
Read more

The Association for Frontotemporal Degeneration (AFTD) HelpLine (866-507-7222) helps people with FTD, families and professionals with information, support and local resources.

🆘 If you’re in crisisFree, confidential support, any time.
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Call or text 988 to reach the 988 Suicide & Crisis Lifeline.

Text HOME to 741741 to reach a trained Crisis Text Line counselor.

If a life is in danger, call 911.
🌍 Outside the U.S.Find free, confidential helplines in your country.
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findahelpline.com lists free, confidential helplines by country. Many countries also have their own Alzheimer’s or dementia association. If you are in danger, call your local emergency number.

📝 Worksheets for this guide

Fill these in privately in the app. Your answers stay on your phone.

What changed firstWhich symptoms came first is one of the biggest clues to the type. Bring these notes to the appointment.
Questions about the diagnosisIt is okay to ask a lot of questions. Write them down before the visit so you don’t forget.
Explaining our diagnosisFind simple words to explain the diagnosis, so friends and family can understand and help.
Good days and bad days diarySome types, especially Lewy body dementia, bring big ups and downs. A short diary helps the care team see patterns.
🔒 Fill in privately in the Mentally United Wellness App. Free, no ads, no accounts.

Sources

  1. National Institute on Aging (NIA), NIH. What Is Dementia? Symptoms, Types, and Diagnosis
  2. National Institute on Aging (NIA), NIH. Lewy Body Dementia: Causes, Symptoms, and Diagnosis
  3. National Institute on Aging (NIA), NIH (2026). Frontotemporal Disorders: Causes, Symptoms, and Diagnosis
  4. Alzheimer’s Association. What Is Alzheimer’s Disease?
  5. Alzheimer’s Association. Vascular Dementia
  6. Lewy Body Dementia Association (LBDA). What Is Lewy Body Dementia?
  7. Lewy Body Dementia Association (LBDA). Lewy Body Dementia Association (Lewy Line)
  8. The Association for Frontotemporal Degeneration (AFTD) (2026). Disease Overview: What Is FTD?
  9. The Association for Frontotemporal Degeneration (AFTD). Contact Us (AFTD HelpLine)
  10. FTD Disorders Registry. FTD Disorders Resources
  11. National Institute of Neurological Disorders and Stroke (NINDS), NIH. Normal Pressure Hydrocephalus
  12. Alzheimer’s Association. 24/7 Helpline
  13. Idaho Commission on Aging. Alzheimer’s Association 24/7 helpline 800.272.3900
  14. 988 Suicide & Crisis Lifeline. 988 Suicide & Crisis Lifeline
  15. Substance Abuse and Mental Health Services Administration (SAMHSA). 988 Suicide & Crisis Lifeline
  16. Crisis Text Line. Crisis Text Line
  17. Substance Abuse and Mental Health Services Administration (SAMHSA). Crisis Text Line (resource listing)
  18. ThroughLine. Find A Helpline
  19. International Association for Suicide Prevention (IASP). If you’re in crisis, help is available right now (Find A Helpline partnership)

This guide is for education and self-care. It is not a diagnosis or a substitute for professional care. Please talk to a counselor or clinical provider about your health. Reviewed October 2026.

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