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For further information, see CMDT Part 24-14: Movement Disorders
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Essentials of Diagnosis
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Any combination of tremor, rigidity, bradykinesia, and progressive postural instability ("parkinsonism")
Cognitive impairment is sometimes prominent
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General Considerations
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Risk factors
Dopamine depletion due to degeneration of the dopaminergic nigrostriatal system leads to an imbalance of dopamine and acetylcholine
Exposure to toxins and certain medications can lead to parkinsonism
Manganese dust
Carbon disulfide
Severe carbon monoxide poisoning
1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine (MPTP) (a recreational drug)
Neuroleptic drugs
Reserpine
Metoclopramide
Postencephalitic parkinsonism is becoming increasingly rare
Only rarely is hemiparkinsonism the presenting feature of a space-occupying lesion
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Common disorder that occurs in all ethnic groups, with an approximately equal sex distribution
The most common variety, idiopathic Parkinson disease, usually begins in people between ages 45 and 65 years
May rarely occur on a familial basis
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Cardinal features
Tremor
Rigidity
Bradykinesia
Postural instability
Nonmotor manifestations include
Affective disorders (depression, anxiety, and apathy)
Psychosis
Cognitive changes
Fatigue
Sleep disorders
Anosmia
Autonomic disturbances
Sensory complaints or pain
Seborrheic dermatitis
Dementia or mild cognitive impairment will eventually develop in many patients
Tremor
Four to six cycles per second
Most conspicuous at rest
Enhanced by stress
Often less severe during voluntary activity
Commonly confined to one limb or to one side for months or years before becoming more generalized
May be present about mouth and lips
May be absent in some patients
Rigidity causes the flexed posture
Bradykinesia is the most disabling symptom, ie, a slowness of voluntary movement and a reduction in automatic movements such as swinging of the arms while walking
The face
Relatively immobile with widened palpebral fissures
Infrequent blinking
Fixity of facial expression
Seborrhea of scalp and face
Mild blepharoclonus
Repetitive tapping (about twice per second) over the bridge of the nose producing a sustained blink response (Myerson sign)
Other findings
Saliva drooling from the mouth
Soft and poorly modulated voice
Variable rest tremor and rigidity in some or all of the limbs
Slowness of voluntary movements
Impairment of fine or rapidly alternating movements
Micrographia
Typically no muscle weakness and no alteration in the tendon reflexes or plantar responses
Difficulty rising from a sitting position and beginning to walk
Gait
Small shuffling steps and a loss of the normal automatic arm swing
There may be unsteadiness on turning, difficulty in stopping, and a tendency to fall
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Differential Diagnosis
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Essential tremor
Depression
Wilson disease
Huntington disease
Normal-pressure hydrocephalus
Multisystem atrophy (previously called Shy-Drager syndrome)
Progressive supranuclear palsy
Corticobasal ganglionic degeneration
Diffuse Lewy body disease
Creutzfeldt-Jakob disease
Drugs causing parkinsonism
Antipsychotic agents
Reserpine
Metoclopramide
MPTP
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