Gilbert syndrome is a syndrome in which the liver of affected individuals processes bilirubin more slowly than the majority. Many people never have symptoms. Occasionally jaundice may occur.
Gilbert syndrome is due to a genetic variant in the UGT1A1 gene which results in decreased activity of the bilirubin uridine diphosphate glucuronosyl transferase enzyme
Rife or Zapper frequencies will assist with symptoms and are effective for many Liver diseases.
Use this set:
1400: Gilbert Disease: 0.08, 0.24, 0.57, 7.5, 12.72, 36.21, 142.5, 321, 415.7, 775.68
in conjunction with this set:
2014: Liver Diseases: 0.2, 0.22, 0.68, 2.45, 3, 7.5, 96.5, 326.16, 505.51, 632.01
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