{"id":13379,"date":"2024-08-23T00:32:56","date_gmt":"2024-08-22T22:32:56","guid":{"rendered":"https:\/\/valintermed.com\/?p=13379"},"modified":"2024-08-23T00:32:56","modified_gmt":"2024-08-22T22:32:56","slug":"sindrom-veylya-markezani","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/veil-markezani-syndrome\/","title":{"rendered":"Weil-Marquesani syndrome"},"content":{"rendered":"
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Weil-Marchesani syndrome (or Marchesani syndrome) is a rare genetic disorder characterized by multiple systemic abnormalities, including skeletal, cardiovascular, and soft tissue abnormalities. It belongs to a group of disorders affecting connective tissue and causes a variety of clinical manifestations, such as high-arched palate, large hands, joint hypermobility, and cardiovascular, pulmonary, and gastrointestinal abnormalities. It is often the first disorder to be diagnosed in children and adolescents, highlighting the importance of early diagnosis and treatment. The prognosis for patients with Weil-Marchesani syndrome varies depending on the severity of clinical manifestations and the extent of organ involvement.<\/p>\n

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