Neuromuscular junction Flashcards
Myasthenia gravis antibodies mediate
post-synaptic acetylcholine receptor
Lamber-Eaton antibodies mediate
block of the pre-synaptic calcium channels
Congenial myasthenia mechanism that affect
presynaptic, synaptic and postsynaptic
Myasthenia gravis clinical
Fatigable weakness in the ocular nerve, limb, truncal
Visual blurring, diplopia, ptosis
Maneuvers in suspected myasthenia gravis
Sustained upgaze: ptosis, medial rectus weakness
Sustained abduction of the arms: patient can no longer hold arms up or weakness
Sustained elevation of leg while supine: can no longer hold leg up or weakness
Repeated arising from chair: fatigues after several attempts
Counting aloud: dysarthria
Differential diagnosis of Myasthenia Gravis. Lamber-Eaton myasthenic syndrome
Sparing ocular muscle, hyporeflexia, dry mouth
Differential diagnosis of Myasthenia Gravis. Congenital myasthenic syndrome
No response to immunomodulation
Differential diagnosis of Myasthenia Gravis. Botulism
Pupillary autonomic involvement
Differential diagnosis of Myasthenia Gravis. Motor neuron disease
Corticoespinal or corticobulbar features, muscle cramps/fasciculations
Differential diagnosis of Myasthenia Gravis. Mitochondrial disorders
No fluctuation, no diplopia
Differential diagnosis of Myasthenia Gravis. Acute immune demyelinating polyneuropathy
No fluctuation in weakness’s sreflexia
Differential diagnosis of Myasthenia Gravis. CNS disorders
Sudden onset, consciousness, coordination and sensation affected, ocular weakness
Differential diagnosis of Myasthenia Gravis. Thyroid ophthalmopathy
Proptosis
ECG in Myasthenia gravis
amplified 3rd wave and low 9th wave
Myasthenia gravis treatment
Anticholinesterases
Immunosuppression
Thymectomy
Corticosteroids