{"id":11071,"date":"2025-07-27T13:26:33","date_gmt":"2025-07-27T11:26:33","guid":{"rendered":"https:\/\/valintermed.com\/?p=11071"},"modified":"2025-07-27T13:26:33","modified_gmt":"2025-07-27T11:26:33","slug":"sindrom-elersa-danlosa-sed","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/elersa-danlosa-sed-syndrome\/","title":{"rendered":"Ehlers-Danlos syndrome (EDS)"},"content":{"rendered":"
<\/div>\n

Ehlers-Danlos syndrome (EDS) is a rare, inherited disorder of connective tissue caused by genetic mutations that impair the synthesis of collagen or its structural components. The clinical features of EDS are variable and may include low blood pressure, increased blood flow to the skin, and increased flatness and elasticity of the skin. The syndrome may manifest as joint hypermobility, hypertelorism, tenderness, and easy bruising, and may involve multiple organ systems including the cardiovascular, musculoskeletal, and skin systems. Over time, the disorder may lead to serious complications, including an increased risk of vascular rupture and joint damage.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n