overview
Frontotemporal dementia is an umbrella term for a group of rare brain disorders that primarily affect the frontal and temporal lobes of the brain. These areas of the brain are generally associated with personality, behavior, and language.
In frontotemporal dementia, parts of these lobes shrink (atrophy). Signs and symptoms vary depending on which part of the brain is affected. Some people with frontotemporal dementia have dramatic personality changes and become socially inappropriate, impulsive, or emotionally indifferent while others lose the ability to use language properly. Frontotemporal dementia Treatment in Nizamabad
Frontotemporal dementia is often misdiagnosed as a psychiatric problem or Alzheimer’s disease. However, frontotemporal dementia tends to occur at a younger age than Alzheimer’s disease. Frontotemporal dementia often begins between the ages of 40 and 65.
symptoms
The signs and symptoms of frontotemporal dementia can vary from individual to individual. The signs and symptoms gradually worsen over time, usually over time.
Groups of symptom types usually appear together, and people can have more than one group of symptom types.
Behavior changes
The most common signs of frontotemporal dementia are extreme changes in behavior and personality. These include:
- Increasingly inappropriate social behavior
- Loss of empathy and other interpersonal skills, such as B. Sensitivity to other people’s feelings
- Lack of judgment
- Loss of inhibition
- Lack of interest (apathy), which can be mistaken for depression
- Repeated compulsive behavior such as knocking, clapping, or smacking your lips
- Decreased personal hygiene
- Changes in eating habits, usually overeating or the preference for sweets and carbohydrates
- Eat inedible items
- Obsessively trying to put things in your mouth
The reasons
In frontotemporal dementia, the frontal and temporal lobes of the brain become narrower. In addition, certain substances accumulate in the brain. The causes of these changes are generally unknown.
There are genetic mutations associated with frontotemporal dementia. But more than half of the people who develop frontotemporal dementia do not have familial dementia.
Recently, researchers have confirmed the genetics and molecular pathways shared between frontotemporal dementia and amyotrophic lateral sclerosis (ALS). However, more research needs to be done to understand the relationship between these conditions. Frontotemporal dementia Treatment in Nizamabad
Risk factors
Your risk of developing frontotemporal dementia is higher if you have familial dementia. No other risk factors are known.