Hypermobility Spectrum Disorder Flashcards

1
Q

What is hypermobility?

A

A pain syndrome in people with joints that move beyond normal limits due to laxity of ligaments, capsules, and tendons

Often referred to as being ‘double-jointed’.

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2
Q

What percentage of the population is affected by hypermobility?

A

10%

Only a few individuals are symptomatic.

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3
Q

In which demographic groups is hypermobility more common?

A

Women and Asian people

Often familial.

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4
Q

At what age does hypermobility usually present?

A

Childhood or young adulthood

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5
Q

What are common symptoms of hypermobility?

A

Pain around the joints, fatigue, and possible recurrent subluxations or dislocations

Pain is worse after activity.

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6
Q

List some other features associated with hypermobility.

A
  • Soft tissue rheumatism (e.g., epicondylitis)
  • Abnormal skin (papyraceous scars, hyperextensible, thin, striae)
  • Marfanoid habitus
  • Arachnodactyly
  • Drooping eyelids, myopia
  • Hernias and uterine/rectal prolapses
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7
Q

What is the main aim of treatment for hypermobility?

A

To improve pain and reduce disability

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8
Q

What is the mainstay of treatment for hypermobility?

A

Non-drug therapy

Focuses on strengthening exercises, posture, and balance.

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9
Q

What are some non-drug therapies for hypermobility?

A
  • Strengthening exercises
  • Work on posture and balance
  • Splinting
  • Surgical interventions may be needed
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10
Q

What pharmacological therapy is recommended for hypermobility?

A

Paracetamol

There is no good evidence base for other medications.

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11
Q

What is the Beighton score?

A

A scoring system to assess hypermobility, with a maximum of 9 points

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12
Q

What is the first maneuver in the Beighton score?

A

Can you put your hands flat on the floor with your knees straight?

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13
Q

True or False: Genetic testing is needed to differentiate between hypermobility spectrum disorder and other connective tissue disorders.

A

True

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14
Q

Name three heritable connective tissue disorders.

A
  • Hypermobility Spectrum Disorder (HSD)
  • Marfan syndrome
  • Ehlers Danlos syndrome
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15
Q

How many subtypes of Ehlers Danlos syndrome are there?

A

13

Each with distinct genetic mutations.

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16
Q

What protein is often defective in Marfan syndrome?

A

Fibrillin

An extracellular matrix protein.

17
Q

What are the most serious complications in Marfan syndrome?

A
  • Ocular complications
  • Cardiac complications (aortic dissection and regurgitation)
18
Q

What is the pathophysiology of hypermobility

A

Due to laxity of ligaments, capsules and tendons
- thought that the origin of the pain is from microtrauma