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Description

Cells 8 , 680 (2019)

Endocrinology 152 , 46104619 (2011)

Best for: Patients in the rebuilding phase of gut healing after the acute inflammation has been addressed and the focus shifts to strengthening and regenerating the mucosal barrier

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