{"id":11976,"date":"2025-04-18T12:18:07","date_gmt":"2025-04-18T10:18:07","guid":{"rendered":"https:\/\/valintermed.com\/?p=11976"},"modified":"2025-04-18T12:18:07","modified_gmt":"2025-04-18T10:18:07","slug":"defitsit-mitohondrialnogo-kompleksa-1","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/mitochondrial-complex-deficiency-1\/","title":{"rendered":"Mitochondrial complex 1 deficiency"},"content":{"rendered":"
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Mitochondrial complex 1 (MK1) deficiency is a rare, inherited disorder that involves dysfunction of the mitochondria, which serve as the cells' energy plants. The defect results in insufficient production of adenosine triphosphate (ATP), which in turn leads to systemic weakness and organ dysfunction. Patients with the disorder may exhibit a variety of symptoms, including muscle weakness, nerve dysfunction, and metabolic disturbances. The disorder is often progressive, and its manifestations vary depending on the patient's age and other individual factors.<\/p>\n

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