Behavioral variant of frontotemporal dementia

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Alternate names[edit | edit source]

Pick disease of the brain; Lobar atrophy of the brain; Dementia with lobar atrophy and neuronal cytoplasmic inclusions; bvFTD; Pick's disease

Definition[edit | edit source]

Pick’s disease is a neurological condition characterized by a slowly progressive deterioration of behavior, personality, or language.

Summary[edit | edit source]

  • People with Pick's disease have abnormal substances (called Pick bodies) inside nerve cells in the damaged areas of the brain.
  • Pick bodies contain an abnormal form of a protein called tau.
  • This protein is found in all nerve cells, but people with Pick's disease have an abnormal amount or type of this protein.

Cause[edit | edit source]

The underlying cause of Pick's disease is unknown.

Inheritance[edit | edit source]

In some cases, the disease runs in families.

Signs and symptoms[edit | edit source]

  • Behavioral variant frontotemporal dementia (bvFTD), involves changes in personality, behavior, and judgment.
  • People with this dementia may have problems with cognition, but their memory may stay relatively intact.
  • They can act strangely around other people, resulting in embarrassing social situations.
  • Often, they don’t know or care that their behavior is unusual and don’t show any consideration for the feelings of others.
  • They may also do impulsive things that are out of character or engage in repetitive behaviors.
  • Over time, language and/or movement problems may occur, and the person needs more care and supervision.

Diagnosis[edit | edit source]

FTD is diagnosed based on symptoms and results of tests, including:

  • Assessment of the mind and behavior (neuropsychological assessment)
  • Brain MRI
  • Electroencephalogram (EEG)
  • Examination of the brain and nervous system (neurological exam)
  • Examination of the fluid around the central nervous system (cerebrospinal fluid) after a lumbar puncture
  • Head CT scan
  • Tests of sensation, thinking and reasoning (cognitive function), and motor function
  • Newer methods that test brain metabolism or protein deposits may better allow for more accurate diagnosis in the future
  • Positron emission tomography (PET) scan of brain
  • A brain biopsy is the only test that can confirm the diagnosis.

Treatment[edit | edit source]

  • There is no specific treatment for FTD.
  • Medicines may help manage mood swings.
  • Sometimes, people with FTD take the same medicines used to treat other types of dementia.
  • In some cases, stopping or changing medicines that worsen confusion or that are not needed can improve thinking and other mental functions.

Medicines include:

  • Analgesics
  • Anticholinergics
  • Central nervous system depressants
  • Cimetidine
  • Lidocaine
  • Medicines may be needed to control aggressive, dangerous, or agitated behaviors.
  • Behavior modification can help some people control unacceptable or dangerous behaviors. This consists of rewarding appropriate or positive behaviors and ignoring inappropriate behaviors (when it is safe to do so).
  • Talk therapy (psychotherapy) does not always work. This is because it can cause further confusion or disorientation.
  • Reality orientation, which reinforces environmental and other cues, may help reduce disorientation.
  • Depending on the symptoms and severity of the disease, monitoring and help with personal hygiene and self-care may be needed. Eventually, there may be a need for 24-hour care and monitoring at home or in a special facility. Family counseling can help the person cope with the changes needed for home care.



NIH genetic and rare disease info[edit source]

Behavioral variant of frontotemporal dementia is a rare disease.


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