Low-Phospholipid Associated Cholelithiasis Report
Low-Phospholipid Associated Cholelithiasis
LPAC is a particular form of biliary lithiasis, in which there is not an excess of cholesterol secretion into bile, but decreased concentrations of phosphatidylcholine, responsible for the formation of stones in the gallbladder and liver. The subjects most at risk are female with a positive family history for gallstones. It manifests itself with intense and intermittent pain in the liver, due to the presence and displacement of the gallstones, even after a long period without symptoms. Genetics plays a key role in the onset of this syndrome, with the ABCB4 and ABCB11 genes at the forefront
3 genes analyzed
It is recommended if:
A genetic test can provide a molecular diagnosis of LPAC syndrome and the screening of high-risk subjects.
List of main conditions:
- Cholestasis, progressive familial intrahepatic 3
- Cholestasis, progressive familial intrahepatic 2
Simple workflow
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