Generalized weakness resident survival guide

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Moises Romo M.D.

Synonyms and Keywords: dystrophy, myasthenia gravis, Guillian-barre syndrome, polymyositis, emg

Overview

Generalized weakness or lack of strength is a direct term for the inability to exert force with ones muscles to the degree that would be expected given the individual's general physical fitness. The weakness may be caused due to affection in the muscle, nerve, or neuromuscular plate. Causes of generalized weakness may be as varied as cardiovascular, chemical, dermatologic, drugs side effects, endocrine, environmental, gastroenterologic, genetic, hematologic, iatrogenic, infectious, musculoskeletal, neurologic, nutritional, oncologic, overdose, psychiatric, and renal. A test of strength is often used during a diagnosis of a muscular disorder before the etiology can be identified. Many times, the cause of weakness may be identified with the history and physical examination; emg may guide into the type of weakness, but other times biopsy or other laboratory test may be necessary.

Causes

Life Threatening Causes

Life-threatening causes include conditions that may result in death or permanent disability within 24 hours if left untreated.

Common Causes

Diagnosis

Shown below is an algorithm summarizing the diagnosis of Generalized weakness according to the American Academy of Neurology guidelines:

 
 
 
Generalized weakness symptoms
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
True motor weakness?
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
No
 
 
 
 
 
Yes
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Evaluate for causes of fatigue or muscle pain
 
Fluctuating
 
 
 
 
 
Constant
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Myasthenia Gravis
Lambert-Eaton syndrome
Periodic paralysis
Metabolic myopathy
 
Acquiered
 
 
 
 
 
Life-long/chronic
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Polymyositis
Dermatomyositis
•Inclusion body myopathy
Amyotrophic lateral sclerosis
Multifocal motor neuropathy
 
Non-progessive
 
 
 
 
 
 
 
Progressive
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Congenital myopathy
Congenital dystrophy
 
Ocular
•Kearns-sayre syndrome
•Oculopharyngeal dystrophy
Ocular dystrophy
 
Facial
•Fascioscapulohumeral dystrophy
Myotonic dystrophy
 
Upper extremities
•Emery-Dreiffus dystrophy
•Hereditary distal myopathy
 
Lower extremities
Duchenne's muscular dystrophy
Becker's muscular dystrophy
Sarcoglycanopathies
Spinal muscular atrophy
•Limb girdle dystrophy


Treatment

Treat the underlying cause.

Do's

  • Inquiere about social history and family history for genetic disorders.
  • Review medications list.
  • Look for upper motor and lower neuron motor signs.
  • Evaluate if weakness is symetrical or asymetrical, as well as for exacerbating factors.
  • Order TSH testing.
  • Order glucose and vitamin B12 deficiency when deficiency is suspected.
  • Order serum and urine testing for drug and toxins exposure.
  • Perform electromyogram and nerve conduction test if lab results are inconclusive.

Don'ts

  • Do not use a muscle biopsy as first testing modality; this should usually be reserved after all other diagnostic workup has failed to reveal a cause.

References

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