{"id":11975,"date":"2025-04-18T12:18:40","date_gmt":"2025-04-18T10:18:40","guid":{"rendered":"https:\/\/valintermed.com\/?p=11975"},"modified":"2025-04-18T12:18:40","modified_gmt":"2025-04-18T10:18:40","slug":"defitsit-mieloperoksidazy","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/myeloperoxidase-deficiency\/","title":{"rendered":"Myeloperoxidase deficiency"},"content":{"rendered":"
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Myeloperoxidase deficiency (MOD) is a rare inherited disorder characterized by a deficiency of myeloperoxidase, an enzyme involved in the formation of reactive oxygen species in neutrophils. This enzyme plays a key role in the immune system, providing protection against pathogens through oxidative reactions. In myeloperoxidase deficiency, neutrophil function is impaired, leading to a reduced ability to fight infections, especially bacterial ones. Clinical manifestations can range from a mild predisposition to infections to severe forms requiring intensive treatment and monitoring. Importantly, this condition can remain undetected for a long time, making diagnosis and timely intervention difficult.<\/p>\n

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