Researchers identify genetic variants and patterns associated with hypermobile Ehlers–Danlos syndrome

Hypermobile Ehlers-Danlos syndrome (hEDS) is one of the most common heritable connective tissue disorders. Early estimates have reported that this genetic disorder affects at least one in 5,000 individuals, and more recently it has been estimated to affect upwards of 1–3% of the population worldwide.

This article was originally published on MedicalXpress.com

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