{"id":12719,"date":"2024-10-11T16:56:13","date_gmt":"2024-10-11T14:56:13","guid":{"rendered":"https:\/\/valintermed.com\/?p=12719"},"modified":"2024-10-11T16:56:13","modified_gmt":"2024-10-11T14:56:13","slug":"fokomeliya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/fokomeliya\/","title":{"rendered":"Phocomelia"},"content":{"rendered":"
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Phocomelia is a rare and serious disorder characterized by abnormal development of the limbs, which may result in the absence of part or all of a limb. The condition can affect both the upper and lower limbs and is often associated with other birth defects, such as facial and organ abnormalities. Phocomelia typically occurs early in embryonic development and can be caused by both genetic and environmental factors, including exposure to toxins and viruses. The condition requires a comprehensive approach to diagnosis and treatment, as it can significantly impact patients' quality of life. <\/p>\n

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