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PubMed Central , Current Opinion in Pharmacology , vol

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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Blood Marker Testing We assess key blood markers to identify inflammation, nutrient deficiencies, and other physiological imbalances that can hinder concussion recovery