What is hypokinesia?
A decrease in bodily movement due to excessive inhibition in basal ganglia circuits, often seen in Parkinson’s disease.
What is hyperkinesia?
An increase in abnormal or involuntary movements caused by insufficient inhibition in basal ganglia circuits, as in Huntington’s disease.
How does the basal ganglia circuitry differ in hypokinetic vs hyperkinetic disorders?
Hypokinetic: overactive indirect pathway and underactive direct pathway → too much thalamic inhibition. Hyperkinetic: loss of inhibitory striatal neurons → reduced indirect pathway activity → excessive thalamocortical drive.
Give two clinical signs of hypokinesia.
Bradykinesia (slowness of movement) and difficulty initiating movement (akinesia).
Give two clinical signs of hyperkinesia.
Chorea (dance-like movements) and dystonia (sustained abnormal postures).
What is the hallmark movement pattern in Parkinson’s disease?
Hypokinetic features: resting tremor, bradykinesia, rigidity, and postural instability.
What is the hallmark movement pattern in Huntington’s disease?
Hyperkinetic features: choreiform, writhing, and fidgety movements.
Where is the primary neurodegeneration located in Parkinson’s disease?
In the dopaminergic neurons of the substantia nigra pars compacta projecting to the striatum.
Where is the primary neurodegeneration located in Huntington’s disease?
In the striatum, especially GABAergic and cholinergic neurons of the caudate and putamen.
How does dopamine change in Parkinson’s disease?
Dopamine levels fall in the striatum due to degeneration of substantia nigra neurons.
What is a Lewy body?
An intracellular inclusion composed mainly of misfolded α-synuclein found in dopaminergic neurons in Parkinson’s disease.
What is the classic clinical triad of Parkinson’s disease?
Resting tremor, bradykinesia, and postural instability (often with rigidity as a key feature).
What is the typical age of onset for Parkinson’s disease vs Huntington’s disease?
Parkinson’s: usually 50–70 years. Huntington’s: usually 30–60 years.
What is the inheritance pattern of Huntington’s disease?
Autosomal dominant with complete penetrance.
Name two major non-motor features that may appear in Parkinson’s disease.
Depression and dementia (plus autonomic symptoms like orthostatic hypotension or constipation).
Describe the imaging hallmark of Huntington’s disease.
Caudate atrophy causing enlargement of the frontal horns of the lateral ventricles; quantified using the bicaudate ratio.
Describe the imaging hallmark often seen in Parkinson’s disease.
Reduced signal in the substantia nigra on MRI and reduced dopamine uptake in the putamen on DAT scans.
What is osteoarthritis (OA)?
A degenerative joint disease where hyaline cartilage wears down, leading to joint space narrowing, osteophytes, and mechanical pain.
What is rheumatoid arthritis (RA)?
A chronic autoimmune inflammatory disease in which synovial tissue proliferates and destroys cartilage and bone.
List three risk factors for osteoarthritis.
Aging, joint trauma/repetitive use, and obesity.
List three risk factors for rheumatoid arthritis.
Genetic susceptibility (HLA-DR), smoking, and being an older adult woman.
How does the pattern of joint involvement differ between OA and RA?
OA: often asymmetric, weight-bearing joints (knees, hips, spine, hands). RA: typically symmetric, small joints of hands and wrists.
How does morning stiffness differ between osteoarthritis and rheumatoid arthritis?
OA: morning stiffness usually < 30 minutes and improves quickly. RA: stiffness > 60 minutes and improves with continued movement.
Describe the key pain pattern for osteoarthritis.
Pain worsens with use and improves with rest.