Ehlers-Danlos Syndrome: Difference between revisions
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== Prevalence == | == Prevalence == | ||
1 | 1 per 5,000 to 1 per 10,000individuals, demonstrating equality males and females of all racial and ethnic backgrounds (Ehlers Danlos National Foundation, Steiner RD emedicine). | ||
== Characteristics/Clinical Presentation == | == Characteristics/Clinical Presentation == |
Revision as of 19:32, 15 February 2010
Original Editors - Students from Bellarmine University's Pathophysiology of Complex Patient Problems project.
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Definition/Description[edit | edit source]
Ehlers-Danlos syndrome is a hereditary collagen disorder characterized by articular hypermobility, dermal hyperelasticity, and widespread tissue fragility (The Merck Manual).
Prevalence[edit | edit source]
1 per 5,000 to 1 per 10,000individuals, demonstrating equality males and females of all racial and ethnic backgrounds (Ehlers Danlos National Foundation, Steiner RD emedicine).
Characteristics/Clinical Presentation[edit | edit source]
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Associated Co-morbidities[edit | edit source]
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Medications[edit | edit source]
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Diagnostic Tests/Lab Tests/Lab Values[edit | edit source]
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Causes[edit | edit source]
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Systemic Involvement[edit | edit source]
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Medical Management (current best evidence)[edit | edit source]
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Physical Therapy Management (current best evidence)[edit | edit source]
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Alternative/Holistic Management (current best evidence)[edit | edit source]
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Differential Diagnosis[edit | edit source]
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Case Reports[edit | edit source]
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Resources
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References[edit | edit source]
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