Lecture 1 - Pathologies PD, MS, MND Flashcards
What is the age of onset for Parkinsons, MS, MND
PD - 60-70
MS - 20-30
MND - 60-70
What is the pathophysiology of PD
widespread degeneration in the CNS, affecting the dopaminergic and non-dopaminergic neural pathways. Many of the motor impairments are due to loss of dopaminergic neurons in the basal ganglia
olfactory part of brain also affected. Multi-system disease.
Neurodegenerative disorder, lose ability to do automated tasks
What is the pathophysiology of MS
An autoimmune condition causing demyelination in the CNS. Resulting impairments are variable and unpredictable depending on the sites off myelin break down.
UMNL or LMNL, disorder of the CNS
myelin sheath breaks down due to an autoimmune response
Pathophysiology of MND
- Degeneration of the Upper and Lower motor neurons. The presenting weakness depends on the location, severity and type of motor neuron involvement effects motor component of brain UMNL or LMNL motor neuron degeneration primary impairment is weakness
Prognosis of MS
near-normal life expectancy
prognosis of MND
6 mo - 5 years (18mo- 3 years?)
Prognosis of PD
near normal life expectancy
Motor Impairments of MS, MND, PD
MS - weakness, lack of coordination (possible cerebellar ataxia), spasticity, impairments depend on location of lesion
MND - weakness, spasticity (if UMNL)
PD - resting/action tremor, bradykinesia, hypokinesia, rigidity, akinesia, postural instability
Sensory Impairments for MS,MND, PD
MS - numbness, visual disturbance, loss of proprioception, increased pain, loss of tactile sensation
MND - no sensation loss
PD - decreased olfactory sensation, decreased taste, pain!, sensory integrative problems (reactive movements)
Cognitive/Emotional Impairments - MS,MND,PD
MND - 20% with UMNL get dementia
MS - 50% develop cog/emo imairments
PD - 80% get dementia within 20 yrs, 25% get cognitive changes on diagnosis - anxiety, depression, apathy
What is Parkinsonism
primary idiopathic PD
parkinsonism plus syndromes
Progressive Supranuclear palsy (PSP)
Mutiple system atrophy (MSA) - brady and hypo, early cog changes
Drug induced parkinsonism
Vascular parkinsonism
4 types of MND
APPP
ALS - Amyotrophic Lateral sclerosis - has UMN and LMN signs - affects bulbar trunk and limbs
PLS - primary lateral sclerosis - isolated UMN signs - affects bulbar, trunk, limb
PMA - Progressive muscle atrophy - isolated LMN signs, - affects bulbar, trunk, and limbs
Progressive Bulbar palsy - UMN and LMN signs - affects bulbar mm
4 Types of MS
Relapse Remitting - 85% initial diagnosis - relapse remit, back to baseline after exacerbation
Secondary Progressive - initial RR course, followed by progression of variable rate, with occasional relapses and minor remissions
Primary Progressive - disease showing progression of disability from onset
Progressive relapse - shows progression from onset, with clear relapses with or without full recovery