I have been diagnosed with a urea cycle disorder (OTC deficiency) featuring episodes of hyperammonemia.
Laboratory Tests @ Quest Diagnostics
• Amino Acid Analysis
• Organic Acids, Full Panel, Quantitative, Urine
• Ammonia, Plasma
Lifecycle -
Fructose consumption leads to the accumulation of fructose-1-phosphate in cells, which may partially deplete intracellular ATP levels in susceptible individuals. Decreased cellular ATP causes disturbances in protein synthesis and reduced ammonia detoxification. Side-effects include fatigue, headaches, dizziness, behavioral changes and depressed immune function (autoimmunity, allergies).
Source: http://www.drkaslow.com/html/fructose.html
Elevated ammonia disrupts energy production in the brain and interferes with communication between neurons (seizures). This damage manifests as sleep disturbances, mood disorders, poor cognition, anxiety, depression and movement disorders (fasciculations). High-protein diets often contribute to high postprandial ammonia levels.
Source: https://www.livestrong.com/article/4765 ... in-damage/
Ornithine Carbamoyltransferase Deficiency - Case 1: After ammonia levels were stabilized, plasma amino acids analysis revealed elevated ornithine, decreased citrulline and elevated glutamine and lysine. Urine organic acids analysis revealed highly elevated urinary orotic acid and a mild urinary uracil peak. A protein-free formula, administered continuously, was gradually changed to increase the dietary protein without a significant rise in serum postprandial ammonia levels.
Source: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342550/
• Test: https://www.invitae.com/en/physician/te ... =CAT000056
Unless it can be proven otherwise, my BFS mystery is solved.