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Lecture On Movement

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Movement Disorders

Movement disorders
Are neurologic syndromes in which
abnormal movements (or dyskinesias)
occur due to a disturbance of fluency &
speed of voluntary movement or the
presence of unintended extramovements
Anatomic & physiologic
consideration
Basal Ganglion: are paired subcortical gray matter
structures that are important in voluntary movements & making
postural adjustment.

They consist of;


Striatum (putamen & caudate)
Globus pallidus (internal & external)
Subthalamic neuclus
Substantial nigra (parscompacta & parsreticula)
BASAL GANGLIA CIRCUITRY
Symptoms of BG diseases
Hyperkinetic movement disorders
an excessive amount of spontaneous motor activity is seen or in which
abnormal involuntary movements occur

Hypokinetic movement disorders


characterized by akenesia or bradykinesia in which purposefull motor
activity is absent or reduced. “Poverty of movement”
HYPOKINETIC
Movement Disorders --
Parkinsonisms
Parkinson’s Disease
Diffuse Lewy Body Disease
Multiple Systems Atrophy (+/- Ataxia)
Progressive Supranuclear Palsy
Corticobasal Degeneration
Vascular Parkinsonism
Post Traumatic Parkinsonism
Secondary (Toxin, Medication, Metabolic)
PARKINSONISMS
Idiopathic Parkinson’s Disease
Usually Asymmetric
Cardinal Signs
– Tremor
– Rigidity
– Bradykinesia
Levodopa Responsive
Later Findings
– Postural Instability
– Levodopa-unresponsive gait disorder
– Non Motor Features (Depression, Sexual Dysfunction,
Cognitive Dysfunction of Variable Severity)
Drug Related Parkinsonism
Antipsychotic medications (typical,
eg.haloperidol) cause symmetric findings
that are indistinguishable at times from
Idiopathic Parkinson’s Disease

Reglan (metoclopromid) is a dopamine


blocker and is an important cause of
Parkinsonism in elderly patients (currently
used as an anti-nausea medication)
HYPERKINESIAS
Hyperkinesias and Dyskinesias
Tremor
Chorea
Dystonia
Myoclonus
Ataxia and Dysmetria
Stereotypies and Tics
Akathisia
Myokymia and Synkinesias
Restless Legs
Periodic Hypnogogic Movements (PLMS)
Movement Disorders -- Tremor
Essential Tremor
– Limbs, Head, Voice
Dystonic Tremor
– Task Specific Tremors
Midbrain Outflow Tremors
– Cerebellar Tremor
– Rubral Tremor
Rest Tremor (Parkinsonism)
Orthostatic Tremor
Exaggerated Physiologic Tremor
– Caffiene, Medication Withdrawal
Other (Drug Related Tremor)
Essential Tremor
Common
Upper Extremity Tremor with Posture and/or
Action
Bilateral, usually roughly symmetric
Typically of Long-Standing Duration
Other Areas May Be Involved
– Head or Jaw
– Voice
– Lower Extremities
Tremor may produce disability, but often doesn’t
No clear association with other diseases or
disorders
Myoclonus
Not a Tremor
Sudden, shock-like muscle contractions
Focal, Multifocal, or Generalized
May be regular and rythmic, but usually
irregular and jerky
Epileptic or Non-Epileptic
– Cortical (Epileptic)
– Brainstem or Spinal Segmental (Non-
Epileptic)
Chorea
Excessive Spontaneous Movements
Irregular, Random, Brief and Abrupt
Non-repetitive
Distal Predominance
Flitting randomly from one body part to another
Purposeless, but may be disguised
(parakinesias)
Facial grimacing and abnormal respiratory
sounds
Chorea -- Causes
MEDICATIONS (e.g. tardive dyskinesia)
– Haldol, other antipsychotics
– Reglan is an important cause of tardive
dyskinesia
Huntington’s Disease
Hemiballism (Stroke)
Post-Infectious (Strep Infection)
Pregnancy
Other Disorders
Tics
Semi-voluntary (e.g. suppressible),
rapid,non-rythmic movements or sounds
Background of normal activity
Associated Compulsions
May be associated with OCD
Occasionally tics are disabling, but the
OCD is usually the more disabling
condition, if it exists
Dystonia
Sustained, patterned muscle contractions
Agonists and Antagonists
Clinical Findings
– Repetitive Twisting or Squeezing Movements
– Fixed Postures
Localization
– Focal
Face (Blepharospasm and Meige Syndrome)
Neck (Cervical Dystonia)
Limbs (Task Specific Dystonias)
– Segmental
– Generalized
Causes of Dystonia
Idiopathic (Most Cases)
DRUG RELATED
– Antipsychotics and Reglan
Genetic (DYT-1 Gene)
Structural
– Trauma
– Stroke
– Multiple Rare Diseases
Ataxia
Symptomatic Interruption of the Cerebellar
Pathways
– Dysmetria (Poor targeting of planned movements)
– Dysdiadochokinesia (Poor sequencing of planned
movements)
– Intention Tremor (Past Pointing)
Gait Abnormalities
– Wide based gait
– Poor balance
“Drunken Sailor’s Walk”
Causes of Ataxia
Lesion in the following areas of the brain
– Cerebellum
– Pons
– Midbrain (Red Nucleus)
– Olivary Nucleus
– Thalamus (Cerebellar Inflow Nucleus)
Causes of Ataxia
Acute intoxication (Alcohol, Dilantin, others)
Chronic Substance Abuse (including Alcohol)
Stroke
Multiple Sclerosis
Brain Tumors
Genetic Ataxias
– Autosomal Dominant Ataxias
– Autosomal Recessive Ataxias
Metabolic
– Vitamin E, Thiamine,
Multiple Systems Atrophy
Treatment of Parkinson’s Disease

Levodopa and Dopamine Agonists

Amantidine, MAO-B Inhibitors

Deep Brain Stimulation (Subthalamic


Nucleus, Globus Pallidus Interna)
Treatment of Dystonia

Artane, Valium, occasionally Baclofen

Botulinum Toxin Injection

Deep Brain Stimulation (Globus Pallidus


Interna)
Treatment of Essential Tremor

Primidone

Propanolol and other Beta Blockers

Deep Brain Stimulation (Thalamus)

Tremors of some patients are quite responsive


to alcohol, and patients may self-medicate
Treatment of Tardive (Post
Dopamine-Blockade) Movement
Disorders
PREVENTION
Dopamine Depleting Agents (Difficult to Obtain
in the U.S.)
Ramp up dopamine blockade (often worsens the
underlying pathologic process)
Life Long Botulinum Toxin Injections
Deep Brain Stimulation
Complications of Dopamine
Blocking Agents
Reversible? Sequelae Include
– Tremor
– Parkinsonism
Permanent and Difficult to Treat Sequelae
Include
– Tardive Dyskinesia (Chorea-like syndrome)
– Tardive Akathisia
– Tardive Dystonia (Long Term Botox, may need DBS)
DEEP BRAIN STIMULATION

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