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Severe cases of homocystinuria are typically caused by autosomal recessive genetic defects and exhibit characteristic clinical features including ocular lens dislocation, marfanoid features and other skeletal abnormalities including osteoporosis, intellectual disability, and thromboembolic disease, the latter frequently being the cause of premature death in affected individuals (28)

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EGCG supplementation improves cognitive performance in animal models by reducing oxidative stress and enhancing memory [44]

Co-regulation of melanin precursors and tyrosinase in human pigment cells: roles of cysteine and glutathione

10.1177/0960327116677355 63 LuC.ZhangF.XuW.WuX.LianN.JinH.et al (2015)

[DOI] [PubMed] [Google Scholar] 81.Yamamoto, M