{"id":12530,"date":"2024-10-11T20:00:38","date_gmt":"2024-10-11T18:00:38","guid":{"rendered":"https:\/\/valintermed.com\/?p=12530"},"modified":"2024-10-11T20:00:38","modified_gmt":"2024-10-11T18:00:38","slug":"pervichnaya-semeynaya-kaltsifikatsiya-mozga","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/primary-family-calcification-of-the-brain\/","title":{"rendered":"Primary familial brain calcification"},"content":{"rendered":"
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Primary familial brain calcification (PFBC) is a rare genetic disorder characterized by abnormal calcification of brain structures, primarily affecting the basal ganglia and subcortical areas of the brain. This condition can manifest itself with various neurological symptoms, including epileptic seizures, cognitive impairment, and movement disorders. PFBC is most often hereditary and can manifest itself in childhood or adolescence, but cases of manifestation in adults have also been reported. Given the neurological nature of the disease, its diagnosis and treatment require a comprehensive approach, including both clinical and laboratory studies.<\/p>\n

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