Ehlers-Danlos syndrome type 3: A rare genetic connective tissue disorder characterized by lax joints, hyperextensible skin and mild connective tissue fragility - a mild form of the condition. More detailed information about the symptoms, causes, and treatments of Ehlers-Danlos syndrome type 3 is available below.
See full list of 9 symptoms of Ehlers-Danlos syndrome type 3
Review possible medical complications related to Ehlers-Danlos syndrome type 3:
Read more about causes of Ehlers-Danlos syndrome type 3.
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Types of Ehlers-Danlos syndrome type 3
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Ehlers-Danlos syndrome type 3 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Ehlers-Danlos syndrome type 3, or a subtype of Ehlers-Danlos syndrome type 3,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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