Week 9: Neurological Disorders Flashcards
What is Alzheimer’s Disease?
A progressive degenerative disorder of the cerebral cortex that accounts for more than one-half of all cases of dementia.
What areas of the brain are affected by Alzheimer’s Disease?
Cortical degeneration is most marked in the frontal lobes, but atrophy occurs in all areas of the cortex.
What is the prognosis for Alzheimer’s Disease?
It is a primary progressive dementia with poor prognosis; most patients die 2 to 20 years after the onset of symptoms, with an average duration of 8 years before death.
What are the two forms of Alzheimer’s Disease?
Familial and Sporadic.
What characterizes Familial Alzheimer’s Disease?
Genes directly cause the disease; it is very rare and has been identified in a relatively small number of families, with many people in multiple generations affected.
What characterizes Sporadic Alzheimer’s Disease?
It is the most common form of the disease; genes don’t cause the disease but may influence the risk of developing it.
What are the four factors thought to contribute to Alzheimer’s Disease?
Neurochemical factors, Viral factors, Trauma, Genetic factors.
What are the distinguishing features of brain tissue in Alzheimer’s patients?
Neurofibrillary tangles, Beta-amyloid plaques, Granulovacuolar degeneration of neurons.
What early cerebral changes occur in Alzheimer’s Disease?
Formation of microscopic plaques and significant atrophy of the cerebral cortex.
How does the presence of beta-amyloid plaques affect dementia severity?
A large number of beta-amyloid plaques results in severe dementia; amyloid may exert neurotoxic effects.
What neurotransmitter is primarily affected in Alzheimer’s Disease?
Acetylcholine; severity of dementia is directly related to its reduction.
What are some complications associated with Alzheimer’s Disease?
Injury from violent behavior, pneumonia, malnutrition, dehydration, and aspiration.
What are the initial signs and symptoms of Alzheimer’s Disease?
Forgetfulness, subtle memory loss, difficulty learning new information, inability to concentrate, and deterioration in personal hygiene.
What symptoms indicate progression of Alzheimer’s Disease?
Difficulty with abstract thinking, progressive communication difficulties, severe memory deterioration, repetitive actions, and mood swings.
How is patient history typically obtained in Alzheimer’s cases?
Almost always obtained from a family member or caregiver.
What is Amyotrophic Lateral Sclerosis (ALS)?
The most common of motor neuron diseases causing muscular atrophy.
What is the typical onset age for ALS?
Onset occurs between ages 40 and 70.
How is ALS characterized?
A chronic, progressively debilitating disease that is rapidly fatal.
What are possible causes of ALS?
Possible causes include a slow-acting virus, nutritional deficiency related to enzyme metabolism, metabolic interference in nucleic acid production by nerve fibers, and autoimmune disorders affecting immune complexes.
What happens to nerve cells in ALS?
Nerve cells that control the muscles, known as motor neurons, are destroyed.
Where are motor neurons located?
Motor neurons are located in the anterior gray horns of the spinal column and the motor nuclei of the lower brain stem.
What occurs as motor neurons die in ALS?
The muscle fibers that they supply atrophy.
What types of motor neurons may be affected in ALS?
Loss of motor neurons may occur in both the upper and lower motor neuron systems.
What is the primary sign of ALS?
Muscle weakness, seen in 60% of affected patients.