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Through advanced testing and a personalized protocol that includes removing the source of exposure, using binders, and implementing therapies such as Phosphatidylcholine IV treatments , he helps patients detoxify and heal

CGD may be caused by variants affecting the core protein gp91 phox (encoded by CYBB ) or one of its subunits ( CYBA , CYBC1 , NCF1 , NCF2 and NCF4 )

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Individuals with moderate glutathione synthetase deficiency may experience symptoms beginning shortly after birth including hemolytic anemia, 5-oxoprolinuria, and elevated acidity in the blood and tissues (metabolic acidosis)