Understanding CPS1 Deficiency: Causes, Symptoms, and Management
Navigating the Complexities of CPS1 Deficiency Cps1 Deficiency, or Carbamoyl Phosphate Synthetase I Deficiency, is a rare but serious genetic disorder affecting the urea cycle. This cycle is crucial for removing ammonia, a toxic waste product, from the body. When the CPS1 enzyme doesn’t function correctly, ammonia builds up in the blood, leading to hyperammonemia. … Read more
