Neuro Differential Diagnosis & Interventions Overview

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Last updated 11:00 PM on 8/22/26
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88 Terms

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Differential Diagnosis

Process of distinguishing between diseases.

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Upper Motor Neuron (UMN)

Nerve cells in the brain that control voluntary movement.

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Lower Motor Neuron (LMN)

Nerve cells that directly innervate muscles.

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Basal Ganglia

Group of nuclei involved in movement regulation.

<p>Group of nuclei involved in movement regulation.</p>
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Cerebellum

Brain region coordinating voluntary movements and balance.

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Hypotonia

Decreased muscle tone, leading to floppiness.

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Hypertonia

Increased muscle tone, often rigid.

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Hyporeflexia

Decreased or absent reflex responses.

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Hyperreflexia

Exaggerated reflex responses, often seen in UMN lesions.

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Clonus

Involuntary muscle contractions and relaxations.

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Babinski Sign

Reflex indicating UMN dysfunction when positive.

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Resting Tremors

Tremors occurring when muscles are relaxed.

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Bradykinesia

Slowness of movement, common in Parkinson's.

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Akinesia

Inability to initiate movement.

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Postural Instability

Difficulty maintaining balance and posture.

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Parkinson's Disease

Progressive disorder from dopamine depletion in substantia nigra.

<p>Progressive disorder from dopamine depletion in substantia nigra.</p>
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Hoehn and Yahr Classification

Stages of disability in Parkinson's disease.

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Stage I

Minimal symptoms, unilateral involvement.

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Stage II

Bilateral symptoms, balance not impaired.

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Stage III

Impaired balance, some activity restrictions.

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Stage IV

Severe symptoms, assistance needed for mobility.

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Stage V

Confined to bed or wheelchair.

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Loss of smell

Early symptom of Parkinson's disease.

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Constipation

Common early symptom in Parkinson's disease.

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Sleep disorders

Sleep-related issues in Parkinson's patients.

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Hypophonia

Soft speech characteristic of Parkinson's disease.

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Mask-like face

Reduced facial expression in Parkinson's patients.

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Micrographia

Small handwriting associated with Parkinson's disease.

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Orthostatic hypotension

Blood pressure drop upon standing.

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Restrictive lung disease

Reduced lung expansion in Parkinson's.

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Dual tasking difficulty

Cognitive challenge in Parkinson's patients.

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Freezing of Gait

Sudden inability to initiate movement.

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Festinating Gait

Shuffling gait with increasing speed.

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En bloc turning

Turning without trunk rotation.

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Levodopa/Carbidopa

Gold standard pharmacological treatment for PD.

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On/off phenomenon

Fluctuations in motor performance with medication.

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Dyskinesia

Involuntary smooth muscle movements during ON phase.

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Dystonia

Muscle contractions causing spasms during OFF phase.

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Multiple Sclerosis

Autoimmune disease causing CNS demyelination.

<p>Autoimmune disease causing CNS demyelination.</p>
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Nystagmus

Involuntary eye movement associated with MS.

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Charcot's Triad

Combination of symptoms in Multiple Sclerosis.

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Lhermitte's Sign

Electric shock sensation down the spine.

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Uhthoff's Phenomenon

Worsening of symptoms with heat exposure.

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Guillain Barre Syndrome

Autoimmune disorder causing rapid nerve demyelination.

<p>Autoimmune disorder causing rapid nerve demyelination.</p>
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Progressive Relapsing MS

Steady disability increase with superimposed attacks.

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Secondary Progressive MS

Initially RR, then continuous symptom increase.

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Primary Progressive MS

Continuous disability increase without attacks.

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Relapse-Remitting MS

Short attacks with full or partial recovery.

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Most common MS type

Relapse-Remitting MS, affecting about 80%.

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MS Exercise Frequency

3-5 times per week, alternating days.

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MS Exercise Intensity

Low intensity, 50-70% VO2, 3-5 METS.

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MS Exercise Duration

30 minutes per session recommended.

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ALS

Progressive neurological disorder affecting motor neurons.

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ALS Symptoms

Muscle atrophy, spasticity, dysphagia, and dysarthria.

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UMN and LMN

Upper and lower motor neuron presentations.

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Pseudobulbar affect

Emotional lability seen in ALS patients.

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Cervical spine extensor weakness

Common in ALS, affecting neck stability.

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Respiratory muscle weakness

Can lead to death in ALS patients.

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GBS Signs

Rapid motor loss, sensory loss, decreased reflexes.

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GBS Recovery Time

Typically 6-12 months, possible full recovery.

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GBS Intervention

Focus on respiratory care and energy conservation.

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Fatigue in ALS

Patients experience easy fatigue during ADLs.

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Medical Management of ALS

No effective treatment; focus on functional activities.

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Energy Conservation Techniques

Recommended to avoid over-fatigue in ALS.

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Cranial Nerve Involvement in GBS

Includes nerves VII, IX, X, XI, XII.

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Sensory Loss Pattern in GBS

Glove and stocking distribution of numbness.

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Presenting Problem

Weird sensations, frequent falls, urination difficulty.

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Family History

Mother has migraines.

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AROM

Active range of motion; grossly intact.

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PROM

Passive range of motion; grossly intact.

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Gait

Slightly wide base of support.

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Tone

Increased tone in biceps, hamstrings, PF.

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Cranial Nerves

Involvement of CN II, III, V, VII.

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Coordination

Impaired coordination observed during evaluation.

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Amyotrophic Lateral Sclerosis

Progressive neurodegenerative disease affecting motor neurons.

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Guillain Barre Syndrome

Autoimmune disorder causing rapid muscle weakness.

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Multiple Sclerosis

Chronic disease affecting central nervous system.

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Cerebellar Tumor

Tumor affecting cerebellum, impacting coordination.

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Pupillary Reflex

Response of pupils to light stimulus.

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Marcus Gunn Pupil

Pupil dilates when light is shone in affected eye.

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Cataract

Clouding of the lens affecting vision.

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Balance Training

Exercises to improve stability and prevent falls.

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Proprioceptive Training

Exercises to enhance body awareness and position.

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Activity Pacing

Adjusting activity levels based on symptoms.

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Pool Therapy Temperature

Recommended water temperature is 87 degrees Fahrenheit.

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Neuro Stroke Class

Scheduled for March 7th at 5 pm PST.

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Non-Systems Classes

Scheduled for March 9th and 12th.

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APC Neuro Masterclass

Free for FLC, 50% off for bundle students.