Alagille Syndrome Precision Panel – 2 genes
The Igenomix Alagille Syndrome Panel can be used to make a directed and accurate differential diagnosis of jaundice in the newborn, for an early initiation of treatment leading to a better prognosis of the disease.
Congenital Hepatic Fibrosis Precision Panel – 6 genes
The Igenomix Congenital Hepatic Fibrosis Gene Panel can be used to make a directed and accurate differential diagnosis of hepatic fibrosis, ultimately leading to a better management of the comorbidities associated with it and a better prognosis of the disease.
Hyperbilirrubinemia Precision Panel – 4 genes
The Igenomix Hyperbilirubinemia Precision Panel can be used to make a directed and accurate differential diagnosis of jaundice, ultimately leading to a better management and prognosis of the disease.
Hemochromatosis Precision Panel – 7 genes
Hereditary hemochromatosis is a condition that results from the body storing an excess of iron. The excess iron is stored in different body organs causing iron overload.
Progressive Familial Intrahepatic Cholestasis Precision Panel – 6 genes
Progressive Familial Intrahepatic Cholestasis (PFIC) is an inherited disorder that causes liver damage in the form of cirrhosis and related symptoms due to the accumulation of bile in the liver.