{"id":11379,"date":"2025-07-26T21:56:49","date_gmt":"2025-07-26T19:56:49","guid":{"rendered":"https:\/\/valintermed.com\/?p=11379"},"modified":"2025-07-26T21:56:49","modified_gmt":"2025-07-26T19:56:49","slug":"defitsit-galaktozoepimerazy","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/galactosidosis-deficiency\/","title":{"rendered":"Galactose epimerase deficiency"},"content":{"rendered":"
<\/div>\n

Galactose epimerase deficiency is a rare genetic disorder that belongs to a group of inherited disorders of carbohydrate metabolism. This condition is caused by a deficiency of the enzyme galactose epimerase, which plays a key role in the metabolism of galactose, one of the main sugars in the body. The lack of this enzyme leads to the accumulation of toxic metabolites, which can cause serious disruptions in the functioning of various organs and systems. Clinical manifestations of the disease can vary from mild to severe, including cognitive impairment, liver damage, cataracts and other complications.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n