Mysathenia Gravis Flashcards
Mys
Muscle
Asthenia
Weakness
Gravis
Serious
What is Mysathenia Gravis?
Autoimmune disease which results from antibodies that block or destroy nicotinic acetylcholine receptors at the junction between the nerve and muscle.
Is MG a Pre-synaptic or Post-synaptic disorder?
Post-synaptic disorder
MG is prevalent in what gender?
Females>Males
Tumor in the thymus
Thymoma
Manifestations for MG
- Weakness and rapid fatigue of any of the muscles under voluntary control.
- Eyes, Face, and Muscles for swallowing
- PTOSIS (CN3) (Ophthalmoplegia)- Drooping of one or both eyelids
- Proximal> Distal Weakness (Mostly affects cervical extensors)
- Decrementing
Response to Exercise - Heat Sensitivity
Drooping of one or both eyelids
PTOSIS- CN3 affectation
Which may be horizontal or vertical, and improves or
resolves when one eye is closed
Diplopia
sustained tight closure of the eyelids can induce fatigue of the orbicularis oculi muscles resulting in the white sclera of the eye slowly becoming apparent under the partially open eye.
Peek Sign
Factors that Can Worsen Myasthenia Gravis
- Fatigue
- Illness
- Stress
- Extreme Heat
- Medications- beta blockers, calcium channel blockers, quinine, and some antibiotics
What do you call about the classification for Myasthenia?
Myasthenia Gravis Foundation of America Clinical Classification Scale
Any ocular weakness
Class 1
Mild Weakness. May also have ocular muscle weakness of any severity.
Class 2