MSK Flashcards

1
Q
  • loss of motor function of the intrinsic hand muscles
  • numbness along inner aspect of hand, forearm, and upper arm
  • total claw hand
  • possible horner syndromer

Most likely d/t injury to

A

Lower trunk of brachial plexus = Klumpke paralysis

MC causes: grabbing something to stop oneself
-delivering a baby w/ arms in the extended position above the head

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2
Q
  • loss of motor function to deltoid ms and teres minor (abduction and lateral rotation)
  • sensory loss in upper lateral portion of arm

Most likely d/t

A

Axillary nerve

  • fracture fo surgical neck of the humerus
  • dislocation of head of the humerus
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3
Q
  • wrist drop
  • loss of motor function to major extensor ms of arm and forearm
  • sensory loss on radial dorsal portion of the hand

Most likely d/t injury to

A

Radial n

  • med humeral fractures
  • saturday night palsy: falls asleep w/ arm over back of chair
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4
Q

MC injury that causes ulnar nerve damage

A

Trauma to elbow (where is passes through cubital tunnel)

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5
Q

Stretching a muscle does what to its passive and active tension

A

Increases passive tension
Decreases active tension

Depends on overlap between actin and myosin:
-stretching a ms decreases degree of overlap and thus decreases active tension force

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6
Q
  • numbness and pain on left aspect of forearm and hand
  • claw hand
  • can raise arm over head
  • decreased radial pulse
  • tx: incision of anterior scalene ms (watch out for phrenic n)

Dx
Borders
What is being compressed

A

Thoracic outlet syndrome

Borders: scalene ms, first rib, clavicle

Compressing: subclavian artery and vein; lower trunk of brachial plexus

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7
Q

Diseases involved in collagen deficiency

A

Scurvy
Osteogenesis imperfecta
Ehlers-Danlos syndromes
Menkes Disease

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8
Q

10 y/o boy presents with

  • hyper-extensible joints
  • frequent joint dislocations
  • easy bruising
  • PE: short for his age, small jaw

Dx
What is abnormal
Mutation

A

Ehlers Danlos

Type 1 Collagen (skin, bone, tendon, vasculature)

PLOD1: encodes enzyme lysyl hydroxylase

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9
Q

X linked recessive dz characterized by

  • sparse, depigmented hair
  • seizures
  • failure to thrive
  • neurodegeneration
  • pts nml die before 10 years of age

D/t mutation that leads to loss of copper distribution

Dx
Mutation

A

Menkes disease

ATP7A

  • copper is needed for many enzymes to function
  • ex. Lysyl oxidase cannot crosslink triple helix collagen molecules
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10
Q

Pt presents w/

  • dislocated lens in one or both eyes
  • defects in aorta: increased risk of aortic rupture
  • tall, slender, w/ elongated fingers and toes

Dx
Defect in
Mutation

A

Marfan syndrome

Defect in elastin

Mutation: fibrillin-1

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