AD3 (medical condition): A degenerative brain disease characterized primarily by progressive dementia. Type 3 has an early onset (starts before the age of 65). It is caused by mutations in the PSEN1 gene which results in the production of a toxic protein (amyloid beta peptide) in the brain which collects into clumps (amyloid plaques) in the brain. These plaques cause damage to nerve cells in the brain.
See also:
Alzheimer disease, familial, type 3:
»Introduction: Alzheimer disease, familial, type 3
»Symptoms of Alzheimer disease, familial, type 3
AD3 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that AD3, or a subtype of AD3,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
AD3: Another name for Alzheimer disease, familial, type 3 (or close medical condition association).
»Introduction: Alzheimer disease, familial, type 3
»Symptoms of Alzheimer disease, familial, type 3
Some of the symptoms of AD3 incude:
See full list of 21 symptoms of AD3 (Alzheimer disease, familial, type 3)
These medical disease topics may be related to AD3:
Source - NIH
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