Acute Hepatic Porphyria Report
$29.00
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Acute Hepatic Porphyria Acute Hepatic Porphyria is due to an enzymatic alteration of porphyrin biosynthesis, which leads to the intratissue accumulation of potentially toxic metabolic by-products. In this form, the deficient enzyme is ALAD, otherwise known as porphobilinogen synthase. 1 genes analyzed It is recommended if: This panel is indicated for those with suggestive clinical and biochemical features of porphyria. The genetic test can also be used to help inform a diagnosis when a patient is not having an acute attack. List of main conditions: Porphyria, acute hepatic
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