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Frontotemporal dementia: changes in personality and speech

Other names: Лобно-височная деменция, disease Пика, изменение характера у человека средних лет, лобная деменция, первичная прогрессирующая афазия, ЛВД

Frontotemporal dementia is a group of diseases in which nerve cells in the frontal and temporal lobes of the brain gradually die. Unlike Alzheimer's disease, it does not begin with forgetfulness, but with changes in personality, behavior or speech, and often at a relatively young age - between 45 and 65 years. A person may become tactless, indifferent to loved ones, impulsive, begin to overeat sweets or commit inappropriate acts without fully realizing the changes. With the speech version, words and understanding of their meaning gradually disappear. Because of this pattern, diagnosis is often delayed and behavior is often considered a character or mental disorder.

🧾 МКБ-10: G31.0 🏥 Where it is treated: 8 Starts with character, not memoryOften up to 65 years of ageThe patient is not aware of the changes
👨‍⚕️ Which doctor
Neurologist, psychiatrist, speech therapist
🔬 Diagnostics
Neuropsychological testing, brain MRI, EEG, TSH, vitamin B12
💊 Treatment
Non-drug behavioral strategies, symptomatic therapy, sessions with a speech therapist, family support
📈 Prognosis
The disease progresses steadily; treatment is aimed at quality of life
⚠️ At risk
Heredity, mutations in certain genes, familial cases of dementia at a young age
⏱ When to see a doctor
Planned

🚨 See a doctor urgently

With these signs do not wait for a scheduled appointment — the condition requires emergency care.

  • Резкое изменение поведения у человека 45–65 лет
  • Утрата чувства дистанции, неуместные поступки, конфликты на работе
  • Быстро нарастающие трудности с подбором слов
  • Опасное поведение: неосторожность на дороге, рискованные траты
  • Появление слабости в руках, подёргиваний мышц, нарушений глотания
  • Судорожные приступы или очаговая неврологическая симптоматика

Forms of the disease

There is a behavioral variant, in which the frontal lobes are primarily affected, and speech variants, associated primarily with the temporal regions. In the behavioral form, personality, motivation, and social skills change. With primary progressive aphasia, the ability to select words and construct phrases or understand their meaning is gradually lost, while memory and orientation are preserved for a long time. Some cases are combined with damage to motor neurons, then muscle weakness, twitching and swallowing disorders are added.

  • Behavioral option - changes in personality and actions
  • Speech Variations—Progressive Aphasia
  • Combination with motor neuron damage
  • Possible features of parkinsonism
  • Hereditary forms with familial accumulation of cases

What does it look like from the outside

Relatives describe that the person has become different: sympathy and interest in the family have disappeared, rudeness, inappropriate jokes, sloppiness, strange habits and stereotypical actions have appeared, food preferences have changed with a craving for sweets. Some patients, on the contrary, become lethargic, lack initiative, and sit around all day doing nothing, which is mistakenly taken for depression. There is no criticism of their condition, so such people are usually brought to the doctor by their relatives.

  • Loss of tact and empathy
  • Impulsive actions and thoughtless spending
  • Apathy and loss of interests
  • Stereotypical repetitive actions
  • Overeating, especially sweets
  • Lack of illness awareness

Diagnostics

The doctor questions the relatives in detail, since the patient himself does not notice the changes. Neuropsychological testing reveals disturbances in the regulation of behavior, planning and speech with relatively intact memory. Magnetic resonance imaging shows selective atrophy of the frontal and temporal lobes, which provides important confirmation. Conditions that give a similar picture must be excluded: depression, bipolar disorder, frontal lobe tumors, hydrocephalus, hypothyroidism, vitamin B12 deficiency, consequences of alcohol abuse. In familial cases, genetic counseling is discussed.

  • Interviewing relatives about behavior changes
  • Neuropsychological testing
  • MRI of the brain with assessment of the frontal and temporal lobes
  • EEG according to indications
  • TSH, vitamin B12, blood biochemistry
  • Psychiatrist consultation
  • Genetic counseling for familial cases

Treatment and care

There are no drugs that stop the death of neurons yet, and drugs used for Alzheimer's disease usually do not help with this form and sometimes increase agitation. Therefore, non-drug approaches become the basis: a structured day, elimination of provoking situations, switching attention, a safe environment. If there is severe impulsiveness and aggression, the doctor may prescribe medications that affect behavior, selecting the minimum effective dose. With speech forms, classes with a speech therapist and auxiliary means of communication - cards, notes, simple phrases - help.

  • Clear daily routine and predictable environment
  • Eliminating situations that provoke conflicts
  • Classes with a speech therapist for speech forms
  • Symptomatic therapy as prescribed by a doctor
  • Control access to money, documents and car
  • Monitoring feeding and swallowing
  • Education and psychological support for families

Practical questions for families

Since the disease often begins during working age, issues of work, finances and legal protection arise early. It is reasonable to discuss in advance with relatives the restriction of access to large sums and execution of transactions, driving issues, and preparation of necessary documents. It is important to explain to those around you that rudeness and indifference are manifestations of illness, and not malicious intent: this reduces tension in the family. Caregivers need rest and support as much as the patient, and it is normal to ask for help.

  • Early resolution of legal and financial issues
  • Stop driving when driving dangerously
  • Explaining the diagnosis to others
  • Division of responsibilities between relatives
  • Support groups and psychological consultations
  • Planning for future care
  • Regular observation by a neurologist

Services and prices for this diagnosis

Based on official price lists of Tashkent clinics. The exact cost is determined after examination.

Frequently asked questions: Frontotemporal dementia (Pick's disease)

Why doesn't a person admit that he is sick?+
When the frontal lobes are damaged, the very ability to critically evaluate one’s behavior suffers. This is a symptom of the disease, not stubbornness. Arguing and convincing is useless; it is more effective to gently redirect attention and organize a safe environment.
How is it different from Alzheimer's disease?+
In Alzheimer's disease, memory for recent events is the first to suffer, but personality persists for a long time. With frontotemporal dementia, the opposite is true: behavior or speech changes first, but memory may be relatively intact. The age of onset is also usually younger.
Is the disease inherited?+
Some cases are hereditary, especially with several cases of dementia at a young age in the family. In such a situation, genetic counseling is indicated. Most cases still occur without a family history.
Do medications help with dementia?+
Medicines that are effective for Alzheimer's disease usually do not work for this form and may increase agitation. There is no proven therapy to stop the disease. Real benefits come from organizing the environment, behavioral approaches, and working with a speech therapist.
Can I continue to work and drive?+
This is decided on an individual basis and is usually limited early because risk assessment and attention are impaired. Safety is more important than your usual routine: discuss the issue with a neurologist and complete the necessary documents in advance.

The information on this page is for reference only and does not replace a doctor consultation. Only a qualified specialist can make a diagnosis and prescribe treatment after an in-person examination.

Where it is treated frontotemporal dementia в Ташкенте

Изменения личности и речи у человека среднего возраста требуют совместной оценки невролога и психиатра. Clinics Ташкента, где принимают эти специалисты:

st. Mirzaeva 50, Yunusabad 17, Yunusabad district, Tashkent Landmark: opposite the Nazar M...
M Turkiston 🚶 1.5 km
M Yunusobod 🚶 2.0 km
M Shahriston 🚶 2.8 km
🚌 Nearest bus stop 🚶 100 m · buses: 7
Mon–Fri:09:00–18:00
Closed now
Branch No. 3: Birlashgan street, opposite the 4-City Clinical Hospital
M Tuzel 🚶 750 m
M Yashnobod 🚶 800 m
M Texnopark 🚶 1.4 km
🚌 Nearest bus stop 🚶 200 m · buses: 22
Пн–Sat:07:00–20:00
Open now
Tashkent, Mirabad district, st. Oybek, 34d
M Toshkent 🚶 550 m
M Oybek 🚶 850 m
M Kosmonavtlar 🚶 1.3 km
🚌 Nearest bus stop 🚶 150 m · buses: 22
Tashkent, A-Yugnaki, st. Proyektnaya, G-40 landmark TTZ, market
🚌 Nearest bus stop 🚶 30 m · buses: 1, 17, 25
Mon–Fri:09:00–17:00
Closed now
Tashkent, Uchtepa district, st. Lutfiy 56d
M Olmazor 🚶 1.8 km
M Chilonzor 🚶 2.0 km
M Mirzo Ulug'bek 🚶 2.7 km
🚌 Nearest bus stop 🚶 20 m · buses: 2, 9Т, 13, 17T, 41, 56
Пн–Sat:08:00–17:00
Closed now
Tashkent, Yakkasaray district, st. Sh.Rustaveli, 109 A
M Oybek 🚶 2.4 km
M Kosmonavtlar 🚶 2.6 km
M Novza 🚶 2.9 km
🚌 Nearest bus stop 🚶 70 m · buses: 2, 11, 12, 40, 45, 47
Пн–Sat:08:00–17:30
Closed now
Tashkent city, Almazar district, st. Kichik Halka Yuli, 5A
M Beruniy 🚶 500 m
M Tinchlik 🚶 1.1 km
M Chorsu 🚶 2.9 km
🚌 Nearest bus stop 🚶 190 m · buses: 31, 34
Mon–Fri:08:30–16:30
Closed now
Tashkent, Olmazar Tumani, Kichik Khalka Yuli 5 "A" y
M Beruniy 🚶 500 m
M Tinchlik 🚶 1.1 km
M Chorsu 🚶 2.9 km
🚌 Nearest bus stop 🚶 190 m · buses: 31, 34
Mon–Fri:08:30–17:00
Closed now

ICD-10 code

Official international classification codes — these are used in medical records and statistics.

Other diseases: Neurology

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