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Alzheimers
disease is the most common cause of dementia in humans.
In Alzheimers
disease, parts of the brain degenerate, destroying cells
and reducing the responsiveness ofthe remaining ones to
many of the chemicals that transmit signals in the brain.
It is
estimated that 4,000,000 people in the United States has
Alzheimers disease and about
47.2% of 85 year old people and older are thought to have
this disease. During autopsy adiseased person that had
suffered from Alzheimers has abnormal tissues,
called senileplaques and neurofibrillary tangles, and
abnormal proteins that appear in the brain.
Alzheimers disease is most associated with
forgetfulness in the elderly. The loss of memory is
usually gradual. Along with memory, thinking, judgment,
and the ability to pay attention and learn are also
impaired. Through examination of a doctor, the diagnosis
of Alzheimers disease is correct 85 % of the time,
but only through an autopsy can Alzheimers disease
be proved through the recognition of abnormal tissues.
One of the largest contributing factors to
Alzheimers disease is thought to be genetic. The
inherited form of this disease has been shown to have
mutations in the presenilin protein 1 and 2, and the
amyloid precursor protein. These disease-linked mutations
result in increased production of the longer form of
amyloid-beta. This site will deal with the presenilin 2
gene.
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