{"id":13186,"date":"2024-08-23T03:46:48","date_gmt":"2024-08-23T01:46:48","guid":{"rendered":"https:\/\/valintermed.com\/?p=13186"},"modified":"2024-08-23T03:46:48","modified_gmt":"2024-08-23T01:46:48","slug":"sindrom-tetra-ameliya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/tetra-amelia-syndrome\/","title":{"rendered":"Tetra-Amelia syndrome"},"content":{"rendered":"
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Tetra-Amelia syndrome is a rare congenital disorder characterized by the complete absence of all limbs in humans. This transposition disorder is one of the most severe variations of aplasia of the upper and lower limbs and is associated with abnormalities in the development of the embryo, resulting in significantly underdeveloped limbs in newborns. The underlying cause of this syndrome is not fully understood, but it is believed to be a combination of genetic predisposition and environmental factors. However, Tetra-Amelia syndrome is often associated with abnormalities in the WNT3 gene, which results in abnormal limb development.<\/p>\n

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