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Central nervous system
Central nervous system


Pick’s disease

Definition:

Pick's disease is a rare and irreversible form of dementia. It causes personality changes, loss of social skills, loss of intellectual function, and speech disturbances.



Alternative Names:
Primary progressive aphasia, Aphasia -- primary progressive; Semantic dementia, Dementia - semantic; Frontotemporal dementia; Arnold Pick's disease

Causes, incidence, and risk factors:

In some ways, Pick's disease is similar to Alzheimer's disease. However, Pick's disease tends to affect only certain areas of the brain, while Alzheimer's can affect any part.

It is the early appearance of a personality changes that help distinguish Pick's disease from Alzheimer’s. (Memory loss is often the main symptom of Alzheimer's.) People with Pick's disease tend to behave inappropriately in different social settings. The changes in behavior continue to get worse and are often one of the most disturbing symptoms of the disease. 

Pick's disease is rare. It is more common in women than men. It may occur in people as young as 20, but usually begins between ages 40 and 60. The average age of onset is 54.

The disease can progress slowly. Over time, the tissues in two parts of the brain (the temporal and frontal lobes) shrink. This shrinking is called atrophy. Symptoms such as behavioral changes, speech difficulty, and impaired intellect occur gradually, but continue to get worse.

People with Pick's disease have abnormalities called Pick bodies and Pick cells inside nerve cells in the damaged areas of the brain. Pick bodies and Pick cells contain an abnormal form of a protein called tau. This protein is found in all nerve cells. But some people with Pick's disease have an abnormal amount or type of tau. The exact cause of these abnormalities is unknown.

A genetic basis for the disease has not yet been determined. Most cases of Pick's disease are not inherited.



References:

Moore DP, Jefferson JW. Handbook of Medical Psychiatry. 2nd ed. St. Louis, MO: Mosby; 2004.

Pierce JM. Pick's disease. J Neurol Neurosurg Psychiatry. 2003 Feb;74(2):169.

Grossman M. Frontotemporal dementia: a review. J Intl Neuropsychol Soc. 2002;8:566-583.

Grossman M. Progressive aphasic syndromes: clinical and theoretical advances. Curr Opin Neurol. 2002;15:1-5.

McKhann G, Albert M, Grossman M, Miller B, Dickson D, Trojanowski J. Clinical and pathological diagnosis of frontotemporal dementia. Arch Neurology. 2001;58:1803-1809.




Review Date: 11/7/2005
Reviewed By: Kevin Sheth, M.D., Department of Neurology, Brigham and Women's Hospital and Massachusetts General Hospital, Harvard Medical School, Boston, MA. Review provided by VeriMed Healthcare Network.

The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. Copyright 2004 A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

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