{"id":11384,"date":"2025-07-26T21:54:07","date_gmt":"2025-07-26T19:54:07","guid":{"rendered":"https:\/\/valintermed.com\/?p=11384"},"modified":"2025-07-26T21:54:07","modified_gmt":"2025-07-26T19:54:07","slug":"defitsit-glyukozo-6-fosfatdegidrogenazy","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/glyukozhozo-6-phosphatdehydrogenase-deficiency\/","title":{"rendered":"Glucose-6-phosphate dehydrogenase deficiency"},"content":{"rendered":"
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Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited disorder associated with a malfunction of an enzyme that plays a key role in glucose metabolism. This enzyme is involved in the process of oxidative phosphorylation and is vital for maintaining NADPH levels, which are necessary for protecting cells from oxidative stress. Patients with G6PD deficiency have increased sensitivity to various factors, including some medications, infectious diseases and certain foods, which can lead to hemolysis of red blood cells and clinical manifestations such as anemia, jaundice and fatigue. The disease has a polyetiological nature and can manifest itself in varying degrees of severity, which makes it an important topic for medical research and practice.<\/p>\n

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