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Barth syndrome (BTHS) is a rare X-linked recessively inherited disorder caused by variants in the TAFAZZIN gene, leading to impaired conversion of monolysocardiolipin (MLCL) into mature cardiolipin (CL)

Helps repair the look of dullness

Gene expression of brain aromatase (Cyp19a1b) and Gonadotropin-releasing hormone (GnRH) is downregulated in a dose-dependent manner

Mitochondria are cellular organelles that perform numerous bioenergetic, biosynthetic, and regulatory functions and play a central role in iron metabolism

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It minimizes the size of the pores on the skin and prevents acne