{"id":11563,"date":"2025-07-26T12:55:04","date_gmt":"2025-07-26T10:55:04","guid":{"rendered":"https:\/\/valintermed.com\/?p=11563"},"modified":"2025-07-26T12:55:04","modified_gmt":"2025-07-26T10:55:04","slug":"gomotsistinuriya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/gomocystinuria\/","title":{"rendered":"Homocystinuria"},"content":{"rendered":"
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Homocystinuria is an inherited disorder associated with a disorder of amino acid metabolism, specifically the inability of the body to process the amino acid methionine. This leads to the accumulation of homocysteine in the body, which can cause a variety of clinical manifestations, including thrombosis, neurological disorders and vascular damage. The disease is usually inherited in an autosomal recessive manner and is associated with mutations in genes involved in the metabolism of folate and vitamin B12. Homocystinuria manifests itself in childhood and adolescence, but severe cases may be diagnosed solely on the basis of characteristic clinical symptoms.<\/p>\n

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