Ehlers-Danlos syndrome type VI: A rare genetic connective tissue disorder characterized by lax joints, scoliosis and fragile sclera of the eye - Ehlers Danlos type with predominant ocular abnormalities. More detailed information about the symptoms, causes, and treatments of Ehlers-Danlos syndrome type VI is available below.
See full list of 25 symptoms of Ehlers-Danlos syndrome type VI
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Ehlers-Danlos syndrome type VI 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 VI, or a subtype of Ehlers-Danlos syndrome type VI,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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