{"id":12204,"date":"2025-01-14T18:20:11","date_gmt":"2025-01-14T17:20:11","guid":{"rendered":"https:\/\/valintermed.com\/?p=12204"},"modified":"2025-01-14T18:20:11","modified_gmt":"2025-01-14T17:20:11","slug":"bolezn-nimanna-pika","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/nimanna-pika-disease\/","title":{"rendered":"Niemann-Pick disease"},"content":{"rendered":"
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Niemann-Pick disease (NPD) is a rare hereditary disorder belonging to the group of lipidoses caused by disorders of lipid metabolism, in particular sphingolipids. The disease is associated with a deficiency of specific enzymes, which leads to the accumulation of specific substances, such as sphingomyelin, in the cells of various tissues of the body. The main manifestations of the disease include neurological disorders, liver and spleen dysfunction, as well as progressive cell degradation, which leads to severe consequences for the health of patients. NPD begins in early childhood, but the form of the disease can vary from type A, which is often fatal, to milder types B and C.<\/p>\n

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