myasthenia gravis is a disease of skeletal muscle acetylcholine receptors;
Occurance;
MG occurs at any age ,involves either men or women;women get it earlier; men get it later.
begin 20-30 commonst age of onset in women;
60-70 commonst in men.
mechanism:
In patients with MG, the antibodies block,alter destroy the receptors for acetylcholine at the neuromuscular junction ,preventing muscle contraction.
factors that aggravates MG:
emotional stress;
sysmetic illness;
thyroid disease;
pregnancy;
menstrual cycle;
fever;
drug.
clinical manifestations:
1.diplopia;
2.blurry vision,difficulty in focus on something;
3.drooping eyelids;
4. dysphagia:difficulty to chew or swallow;
5.dysphonia:voice impairment;
6.cessation of activities that requres prolonged use of muscles;
most of patints with myathenia gravis present with ocular manifestation.
65% patients :ptosis or diplopia;
17% :patients:oropharygeal muscle weakness; (difficulty in chewing and swallowing)
10% limb weakness.
(from harvard PPT)
Myopathy Myasthenia Symmetric Appearance Asymmetric No Ptosis on fatigue Yes No Lid twitch Yes No Recovery w/ eye closure Yes Constant Range lev. function Varies Yes Weak orb. oculi Yes Negative Tensilon test Positive 50% Family history Rare Slowly Progressive Course Fluctuates
severity of weakness fluctuates during the day:
least in the moring ,worsening as the day progress ,especally after prolonged use of affected muscles.
classfication:
1.ocular alone;
2.mild generalized;????
3.moderately severe generalized plus usually bulbar involvement;
4.acute severe over weeks-months with severe bulbar involvement;
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