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PLC hydrolyzes phosphatidylinositol 4,5-P(PIP) into 1,2-diacylglycerol (DAG) and inositol 1,4,5-triphosphate (IP)

X-linked recessive: 5 defects which are X-linked- CHO (G6PD deficiency) Lipid metabolism (Fabry's disease, caused by Alpha Galactosidase, which is X-linked recessively inherited) Amino acid metabolism (Type 2 Hyperammonemia) Puri Salvage metabolism- GPRTase defect, which is an enzyme of the Purine Salvage pathway, and the Defect of this enzyme causes Lesch Nyhan Syndrome

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This characteristic is essential for encouraging fat reduction and preserving metabolic balance

Vegetable Capsule (Hypromellose) Vegan-friendly, ensuring broader compatibility for patients