Generalized weakness resident survival guide

Revision as of 12:38, 22 October 2020 by MoisesRomo (talk | contribs)
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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
•Dematomyositis
•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
•Fascioscapulohumarl 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

  • The content in this section is in bullet points.

Don'ts

  • The content in this section is in bullet points.

References

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