Homocystinuria

Homocystinuria is a rare genetic metabolic disorder characterized by an abnormal buildup of homocysteine in the blood and urine. It results from deficiencies in enzymes involved in the metabolism of methionine, an amino acid. The most common cause is a deficiency of the enzyme cystathionine beta-synthase (CBS), which converts homocysteine into cystathionine, which further leads _________ _______ ______ ___ ____ ______ __________ _________ ______ ________ _____ ________.
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