Tag: Hcu diet

For individuals with homocystinuria (HCU), managing symptoms is directly tied to diet, as a build-up of homocysteine and methionine can be toxic. A primary treatment strategy is a restricted low-protein diet to control methionine intake. This article explains exactly what should be reduced in diet for Homocystinuria and how to manage this complex nutritional plan.

Classic homocystinuria, or HCU, is a rare genetic disorder affecting about 1 in 200,000 births, impacting the body's ability to process the amino acid methionine. A lifelong, low-methionine diet is the cornerstone of managing this inherited metabolic condition and preventing serious health complications.