{"id":13436,"date":"2024-08-22T23:35:50","date_gmt":"2024-08-22T21:35:50","guid":{"rendered":"https:\/\/valintermed.com\/?p=13436"},"modified":"2024-08-22T23:35:50","modified_gmt":"2024-08-22T21:35:50","slug":"h-stseplennaya-displaziya-klapanov-serdtsa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/h-septal-displasia-of-the-heart-valves\/","title":{"rendered":"X-linked cardiac valvular dysplasia"},"content":{"rendered":"
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X-linked valvular dysplasia is a rare inherited disorder characterized by abnormal development of the heart valves and their structures. The condition is associated with mutations in genes located on the X chromosome, which leads to disruption of the normal formation and function of the heart valves. Dysplasia can manifest itself in various clinical manifestations, including stenosis or regurgitation of the valves, which in turn can lead to serious cardiovascular disorders. Since the disease more often affects men, it may manifest itself in a milder form in women or remain asymptomatic. Timely diagnosis and competent treatment of this condition are key factors in achieving a favorable prognosis.<\/p>\n

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