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Myasthenia Gravis (Pauly - 14 points) – Questions And Verified Answers $10.49   Add to cart

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Myasthenia Gravis (Pauly - 14 points) – Questions And Verified Answers

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Myasthenia Gravis (Pauly - 14 points) – Questions And Verified Answers

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  • August 13, 2024
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  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • MYASTHENIA GRAVIS
  • MYASTHENIA GRAVIS
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Myasthenia Gravis (Pauly - 14 points) – Questions And
Verified Answers

Myasthenia Gravis Right Ans - grave muscular weakness

Chronic autoimmune Right Ans - neuromuscular (junction) disorder

History of Right Ans - fatiguable weakness & recovery with rest

Rare, affects Right Ans - all people regardless of age, race, ethnicity, family
history
since autoimmune, is genetic predisposition but MG not directly hereditary

Variable weakness in skeletal muscle Right Ans - ocular, bulbar, limb, and
respiratory

Selective vulnerability Right Ans - muscle weakness in eyes, eyelids,
shoulder, hip, diaphragm, neck, chewing/swallowing muscles

Muscle weakness results in Right Ans - double vision, obstruction of vision,
trouble chewing/swallowing, talking, breathing, and dysfunction of arms/legs

Generalized disease Right Ans - weakness affects ocular muscles and
variable combo of bulbar, limb, and respiratory

Most severe type of MG Right Ans - generalized: due to involvement of
respiratory muscles

Ocular myasthenia Right Ans - weakness limited to eyelids/extraocular
muscles

Neonatal MG Right Ans - transient form - mother has MG and passes
antibodies to baby
breast feeding can transfer antibodies
usually subsides once antibody transmission stopped (birth)

, Congenital MG Right Ans - non-autoimmune related, caused by an issue
than occurred during development

Ptosis Right Ans - drooping of one or both eyelids

Diplopia Right Ans - double vision

Bulbar Right Ans - face and throat muscles
- difficulty chewing, limited facial expressions

Dysarthria Right Ans - altered speaking

Dysphagia Right Ans - difficulty swallowing

Neck and limb muscles Right Ans - weakness in arms, fingers, legs

Myasthenic Crisis Right Ans - weakness in chest muscles
most serious, affects respiratory

Symptoms Right Ans - worsen throughout the day and improve with rest

Early symptoms are transient Right Ans - take weeks-months to progress

Symptoms peak Right Ans - ~2 years (active stage)

Diagnosis Right Ans - Ice pack test
Tension test
Serological tests
Repetitive nerve stimulation
Thymus imaging

Ice pack test Right Ans - one of main diagnosis tests
2-5 mins with ice pack on eye (only ptosis)
*cooling improves neuromuscular transmission

Tension test (edrophonium) Right Ans - increase in muscle strength
NO LONGER USED due to false positives
-short 1/2 life AChEi IV

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