Myasthenia gravis history and symptoms: Difference between revisions

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==History==
==History==


==Symptoms==
==Common symptoms==


The hallmark of myasthenia gravis is Fluctuating [[weakness]] of specific [[Muscle|muscles]] in [[limbs]], [[bulbar]], [[ocular]] and [[respiratory system]] which get worse with activity or using the muscle.(1-2 clinical va 63 symptom asli)  
Symptoms of myasthenia gravis include:
===== ptosis and diplopia =====
About 50 percent of patiens have [[ptosis]] and [[diplopia]] as their presenting sign. [[Ptosis]] is usually asymmetrical. The direction and degree of [[diplopia]] may change in a [[Myasthenia gravis|MG]] patients because of [[Fatigue|fatigable]] [[ocular]] motor [[paresis]].(10 uptodate ocular)
===== Gaze paralysis =====
The [[Ocular muscles|ocular muscle]] [[weakness]] in [[Myasthenia gravis|MG]] can cause [[Gaze palsy|gaze paralysis]] and even mimic [[internuclear ophthalmoplegia]] or midline [[brain]] lesions.(146 asli)


==References==
==References==

Revision as of 05:16, 22 June 2018

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Overview

History

Common symptoms

The hallmark of myasthenia gravis is Fluctuating weakness of specific muscles in limbs, bulbar, ocular and respiratory system which get worse with activity or using the muscle.(1-2 clinical va 63 symptom asli)   Symptoms of myasthenia gravis include:

ptosis and diplopia

About 50 percent of patiens have ptosis and diplopia as their presenting sign. Ptosis is usually asymmetrical. The direction and degree of diplopia may change in a MG patients because of fatigable ocular motor paresis.(10 uptodate ocular)

Gaze paralysis

The ocular muscle weakness in MG can cause gaze paralysis and even mimic internuclear ophthalmoplegia or midline brain lesions.(146 asli)

References

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