{"id":12684,"date":"2024-10-11T17:32:41","date_gmt":"2024-10-11T15:32:41","guid":{"rendered":"https:\/\/valintermed.com\/?p=12684"},"modified":"2024-10-11T17:32:41","modified_gmt":"2024-10-11T15:32:41","slug":"sindrom-pottera","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/potter-s-syndrome\/","title":{"rendered":"Potter syndrome"},"content":{"rendered":"
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Potter syndrome is a rare but serious condition that is a group of abnormalities that result from inadequate development or absence of the kidneys, leading to significant developmental disabilities in the fetus. The condition is associated with both a lack of urine and a deficiency of amniotic fluid, which can ultimately lead to severe abnormalities in the lungs and other organs. The condition is characterized by a specific appearance of the newborn, including deformities of the face, limbs, and ear placement. The main cause of Potter syndrome is the absence or underdevelopment of the kidneys (renal agenesis or hypoplasia), which creates the conditions for the development of the so-called "amniotic fluid deficiency syndrome."<\/p>\n

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