{"id":11311,"date":"2025-07-27T01:30:03","date_gmt":"2025-07-26T23:30:03","guid":{"rendered":"https:\/\/valintermed.com\/?p=11311"},"modified":"2025-07-27T01:30:03","modified_gmt":"2025-07-26T23:30:03","slug":"bolezn-goshe-3-go-tipa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/sick-goshe-3-go-type\/","title":{"rendered":"Gaucher disease type 3"},"content":{"rendered":"
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Gaucher disease type 3, or the neurogenerative form of the disease, is a rare inherited disorder associated with a deficiency of the enzyme glucocerebrosidase, which leads to the accumulation of glucocerebrosides in various tissues and organs. This leads to damage to the nervous system and pronounced systemic manifestations. Unlike the more common Gaucher disease type 1, in which neurological symptoms are absent or mild, type 3 is characterized by progressive neurological damage that usually becomes noticeable in childhood or adolescence. This form of the disease has a complex pathogenesis and can cause serious complications affecting both the central and peripheral nervous systems.<\/p>\n

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