𝐯𝐄𝐃𝐒 (𝐕𝐚𝐬𝐜𝐮𝐥𝐚𝐫 𝐄𝐡𝐥𝐞𝐫𝐬-𝐃𝐚𝐧𝐥𝐨𝐬 𝐒𝐲𝐧𝐝𝐫𝐨𝐦𝐞) is an uncommon, dominantly inherited, genetic connective tissue disorder. vEDS is rare and patients usually have a very characteristic appearance to their face and skin (skin is very translucent and veins are very prominent). Vascular Type EDS is considered the most serious form of EDS due to the possibility of arterial or organ rupture. Although joint hypermobility occurs, it is much less prominent in vEDS than the other more common types and is mainly confined to the hands.
The Center for Complex Neurology, EDS & POTS is dedicated to caring for patients with complex neurological problems, including Vascular Ehlers-Danlos Syndrome. EDS is often an invisible disability and it is important to have the right physicians in your corner. Dr. Saperstein has cared for thousands of patients with EDS. He and his team at the Center provide care for the numerous complications of EDS.
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