neuromuscular conditions (gbs,mnd)

  • types of NMD

    • neuropathies

      • GBS

      • chronic inflammatory demyelinating polyneuropathy

      • Charcot Marie tooth disease

    • motor neuron diseases

      • ALS

      • primary lateral sclerosis

      • spinal muscular atrophy

    • neuromuscular junction disorders

      • myasthenia gravis

    • myopathies

      • muscular dystrophies

  • Guillain-barre syndrome

    • pathogenesis

      • acute polyneuropathy (immune mediated)

        • demyelination

        • axonal degeneration (in severe cases)

    • what causes it

      infections like campylobacter jejuni, causing gastro. also infection like HIV, influenzas and zika virus

    • clinical features of GBS

      • progressive bilateral weakness, initially in LL

      • paraesthesia: numbness and tingling

      • pain - diffuse

      • autonomic dysfunction: postural hypotension, arrhythmias

      • may involve swallowing issues and respiratory muscle issues

    • more likely in men or women

      men, 2:1

    • drug therapy

      • plasmaphoresis

      • immunoglobin infusion

    • physio role

      • prevent secondary impairments like

        • cardiorespiratory complication s

        • maintain muscle strength and length

        • prevent skin breakdown, DVT’s

    • exercise prescription

      • strength training

        • submax suggested

        • increase reps before load

        • do fast twitch training

      • aerobic exercise

        • may not improve fatigue or function

        • moderate intensity

  • motor neuron disease

    • pathogenesis

      • progressive degeneration of motor neurons

        • sensory system is generally spared

    • diagnosis

      • clinical diagnosis

      • exclude other conditions

      • upper and lower motor neuron signs and progression of disease

    • clinical features

      • LMN: progressive bulbar palsy,

        • weakness

        • atrophy

        • cramps

        • fasciculations

        • hyporeflexia

        • hypotonicity

      • UPM

        • weakness

        • spasticity

        • hyperreflexia

        • pseudobulbar affect

      • upper and lower: ALS (amyotrophic lateral sclerosis)

        • dysarthria

        • dysphagia

        • fatigue

        • respiratory insufficiency

    • drug therapy

      no major effect on disease progression

      symptoms management

    • evidence on exercise

      • insufficient exercise on whether or not it is beneficial

      • some to show it helped improve ALS functional rating scale

functional nerurological disorder - its own thing 

  • what is FND

    a disorder of motor and sensory symptoms (paralysis, tremor and seizures) that are genuinely experienced and related to a functional rather than a structural disorder

  • diagnosis

    • exclude other structural disorders

    • made by neurologist and psychiatrist

    • usually triggered by an underlying psychological trigger