Homocystinuria: Causes, Symptoms, Diagnosis, and Treatment
Homocystinuria is a rare genetic disorder characterized by the inability of the body to properly process the amino acid methionine. It results from mutations in…
Drug-induced pyridoxine deficiency
Pyridoxine, also known as vitamin B6, is a vital nutrient involved in numerous physiological processes, including amino acid metabolism, neurotransmitter synthesis, and immune function. Drug-induced…