Hypermobile EDS with postural orthostatic hypotension - search for identification of large kindreds.
Few disorders are more challenging than hypermobile Ehlers-Danlos Syndrome (formerly known as EDS type III) when trying to identify cause. Defining a population of patients with a clear clinical phenotype is an essential first step. We are actively recruiting individuals with hypermobile EDS and postural orthostatic hypotension (changes with blood pressure on standing or known abnormalities in autonomic testing) to recruit families with multiple affected family members with hypermobile EDS with or without autonomic alteration. The nature of the families and the number of individuals available will determine how each study is done. We will need detailed clinical information, may ask affected individuals to be seen in the Genetic Medicine Clinic at the University of Washington, and collect a blood sample to complete the study."
Contact information: Dru Leistritz, MS, CGC (dru2@uw.edu)
Thanks! We're rather far from Washington, but I'll definitely look into this for me and my kids!
ReplyDeleteHi! Great blog! Is it possible to have POTS if you do not have an increase of 30 bpm within 10 minutes of standing up ? I have most symptoms of POTS, yet I do not have tachycardia. My pulse increase around 20-25 bpm within standing up.
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