{"id":12150,"date":"2025-03-13T20:21:54","date_gmt":"2025-03-13T19:21:54","guid":{"rendered":"https:\/\/valintermed.com\/?p=12150"},"modified":"2025-03-13T20:21:54","modified_gmt":"2025-03-13T19:21:54","slug":"sindrom-melas","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/melas-syndrome\/","title":{"rendered":"MELAS syndrome"},"content":{"rendered":"
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MELAS syndrome (mitochondrial encephalopathy, lactic acidosis and stroke-like episodes) is a rare inherited disorder characterized by multiple disorders of the nervous system and other organs caused by mitochondrial dysfunction. The main clinical manifestations include neurological disorders such as migraines, stroke episodes, and metabolic disturbances including hyperlactacidemia. Developmental delay, progressive muscle weakness, and organ damage such as the heart and kidneys are also common. MELAS syndrome usually has a progressive course and remains a disease with high morbidity and mortality at a young age.<\/p>\n

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