Ehlers-Danlos Syndrome Flashcards

1
Q

what is EDS

A

inherited connective tissue disorders which affect one’s skin, joints, and blood vessels

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2
Q

how is EDS passed genetically

A

autosomal dominant
or
autosomal recessive

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3
Q

what are the characteristics of EDS

A

hyperelasticity
hypermobility
atrophic scarring
tissue fragility

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4
Q

what is a common disorder found in those with EDS

A

POTS

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5
Q

EDS common s/s

A

hypermobility
joint pain
dislocation
early OA onset
soft velvety skin

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6
Q

prognosis of EDS

A

no available cure and treatment is tailored to individual symptoms

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7
Q

which form of EDS has the worst prognosis

A

vascular EDS

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8
Q

what scale can be used to help diagnose EDS

A

beighton scale
– >5/9 = positive

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9
Q

what pain management techniques are used in EDS populations

A

soft tissue mobilization
myofascial release
chronic joint pain

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10
Q

what to avoid with those that have EDS

A

high impact resistance training
hyperextension

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11
Q

what can be done in joints that are lax

A

proprioception exercises

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12
Q

when is surgery indicated?

A

address joint damage due to dislocation
– can have poor outcomes postop due to tissue deficits

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13
Q

what can assistive technology assist with in EDS populations

A

increase joint stability and decrease likelihood of dislocation
- walking, loading LE, balance

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