Motor Disorders Flashcards
What is Huntington’s disease?
A neurodegenerative disorder involving affective, cognitive, and motor symptoms.
What gene is responsible for Huntington’s disease?
A mutated version of the huntingtin (HTT) gene on chromosome 4.
What does it mean that the HTT gene is autosomal dominant?
Offspring of a person with this gene have a 50% chance of inheriting the disease.
Which areas of the brain are affected by Huntington’s disease?
Caudate nucleus, putamen, cerebral cortex, cerebellum, and thalamus.
What neuroimaging findings are associated with Huntington’s disease?
Glucose hypometabolism and atrophy in the caudate nucleus and putamen.
What neurotransmitters are associated with Huntington’s disease?
GABA, dopamine, and glutamate.
At what age do symptoms of Huntington’s disease most often appear?
Between 30 and 50 years of age.
What is the typical life expectancy following the onset of symptoms in Huntington’s disease?
10 to 30 years.
What are the early affective symptoms of Huntington’s disease?
Depression and mood swings.
What cognitive symptoms are associated with Huntington’s disease?
Short-term memory loss and impaired concentration and judgment.
What is the primary motor symptom of Huntington’s disease?
Chorea, involving irregular, uncontrollable jerky or writhing movements.
What severe motor symptoms occur in the later stages of Huntington’s disease?
Rigidity and bradykinesia, trouble walking, speaking, and swallowing.
What criteria may a person with advanced Huntington’s disease meet?
Criteria for mild or major neurocognitive disorder.
Is there a cure for Huntington’s disease?
No, there is no cure.
What are the goals of treatment for Huntington’s disease?
To relieve symptoms and improve quality of life.
What is Parkinson’s disease?
A neurodegenerative disorder that produces prominent motor symptoms due to a combination of genetic and environmental factors.
What causes the motor symptoms in Parkinson’s disease?
Degeneration of dopamine-producing cells in the substantia nigra, reducing dopamine levels in areas of the basal ganglia.
What role does excessive glutamate activity play in Parkinson’s disease?
It is implicated in the progression of the disease.
How do low levels of acetylcholine (ACh) affect individuals with Parkinson’s disease?
They contribute to impairments in gait, balance, and cognitive decline.
What non-motor symptoms are associated with low levels of norepinephrine in Parkinson’s disease?
Depression, cognitive deficits, sleep disturbances, and other non-motor symptoms.
What genetic variant is linked to an increased risk for neurocognitive disorders in Parkinson’s disease?
Variants of the ApoE gene.
List the primary motor symptoms of Parkinson’s disease.
What is a resting tremor in Parkinson’s disease?
A tremor that occurs when muscles are at rest, beginning in the hands and including ‘pill rolling’.
What is postural instability?
Impaired balance and coordination.