{"id":11299,"date":"2025-07-27T01:59:33","date_gmt":"2025-07-26T23:59:33","guid":{"rendered":"https:\/\/valintermed.com\/?p=11299"},"modified":"2025-07-27T01:59:33","modified_gmt":"2025-07-26T23:59:33","slug":"fukozidoz","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/fukozidoz\/","title":{"rendered":"Fucosidosis"},"content":{"rendered":"
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Fucosidosis is a rare genetic disorder belonging to the group of lysosomal storage diseases associated with the absence or decreased activity of the enzyme fucosidase. This leads to the accumulation of fucosyl-containing polysaccharides in cells, which has a negative effect on the organs and systems of the body, especially the liver, spleen and bone marrow. The pathology can manifest itself in early childhood, leading to growth retardation, disruption of the functional activity of organs and systems, as well as a number of other significant complications.<\/p>\n

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