{"id":11228,"date":"2025-07-27T05:27:09","date_gmt":"2025-07-27T03:27:09","guid":{"rendered":"https:\/\/valintermed.com\/?p=11228"},"modified":"2025-07-27T05:27:09","modified_gmt":"2025-07-27T03:27:09","slug":"semeynyy-defitsit-glyukokortikoidov","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/family-glyukokortikoidov-deficiency\/","title":{"rendered":"Familial glucocorticoid deficiency"},"content":{"rendered":"
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Familial glucocorticoid deficiency (FGCD) is a rare inherited disorder characterized by insufficient production of glucocorticoids by the adrenal glands. This condition may occur due to a disorder in the synthesis of cortisol, which leads to a variety of clinical manifestations, including weakness, fatigue, low blood pressure, hypoglycemia, and fluid and electrolyte disturbances. The pathology is most often diagnosed in childhood or adolescence, but early symptoms may not be obvious. Cortisol deficiency can significantly affect the metabolism, immune response, and overall health of the patient, which requires careful diagnosis and timely treatment.<\/p>\n

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