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Previous studies have shown that hereditary oxalate deposition disorder, characterized by CaOx nephrolithiasis, renal failure, and oxalate crystal deposits in various tissues and organs throughout the body, is an inborn defect in glyoxylate metabolism

Cleansing is often underestimated, but it plays a key role in how skin looks

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Mohan R , Kabir T, Wu AGR, Lim KI, Goh BKP

The riboflavin deficiency will reduce the synthesis of active riboflavin adenine dinucleotide, impair hydrogen delivery of erythrocytes, reduce glutathione reductase, and weaken the activity of erythrocyte glutathione reductase, thus aggravating hemolysis (Wang et al., 2021)