MSK Flashcards
- 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
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
- 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
Axillary nerve
- fracture fo surgical neck of the humerus
- dislocation of head of the humerus
- 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
Radial n
- med humeral fractures
- saturday night palsy: falls asleep w/ arm over back of chair
MC injury that causes ulnar nerve damage
Trauma to elbow (where is passes through cubital tunnel)
Stretching a muscle does what to its passive and active tension
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
- 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
Thoracic outlet syndrome
Borders: scalene ms, first rib, clavicle
Compressing: subclavian artery and vein; lower trunk of brachial plexus
Diseases involved in collagen deficiency
Scurvy
Osteogenesis imperfecta
Ehlers-Danlos syndromes
Menkes Disease
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
Ehlers Danlos
Type 1 Collagen (skin, bone, tendon, vasculature)
PLOD1: encodes enzyme lysyl hydroxylase
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
Menkes disease
ATP7A
- copper is needed for many enzymes to function
- ex. Lysyl oxidase cannot crosslink triple helix collagen molecules
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
Marfan syndrome
Defect in elastin
Mutation: fibrillin-1