Ehlers-Danlos syndrome

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Background

  • Hereditary connective tissue disorder
  • Six types: Classic, hypermobility, vascular, kyphoscoliosis, arthrochalasia, dermatosparaxis

Clinical Features

  • Hyper-extensible skin, classically "doughy" or "velvety"
  • Hypermobile joints
  • Tissue fragility and poor wound healing

Increased risk of:

Differential Diagnosis

  • Marfan syndrome
  • Cutis laxa
  • Loeys-Dietz syndrome
  • Osteogenesis imperfecta
  • Larsen Syndrome
  • Stickler syndrome
  • Arteria tortuosity syndrome

Evaluation

Management

  • Cardiac evaluation to screen for valvular disease, vascular disease, and aortic aneurysm
  • Ophthalmologic evaluation to screen for myopia, retinal detachment, and glaucoma
  • Monitoring of skin fragility, wound healing, easy bruising

See Also

External Links

References