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PPAR is able to upregulate the expression of almost all genes involved in the carnitine shuttle mechanism (e.g., CPT1, CPT2, CACT and CrAT) [193, 194]
LaValle, RPh, CCN, MT pp 32-39)
Possible Deficiency Poor wound healing Reduced taste or smell Hair loss or skin changes Frequent infections Reduced appetite Higher-Risk Conditions Chronic diarrhea Celiac or inflammatory bowel disease Bariatric surgery Restricted or low-protein diets Alcohol-related or chronic illness Walsh and Copper Evaluation Copper overload concerns Pyroluria assessment Anxiety or mood symptoms with suspected mineral imbalance Monitoring zinc treatment Broader biotype testing Should Copper and Ceruloplasmin Also Be Tested
Genetic counselors can answer your questions about how CAT deficiency is inherited, options during future pregnancies, and how to test other family members
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