Acute intermittent porphyria (AIP) is a rare, genetic disorder characterized by abnormalities in the production of hemoglobin, the oxygen-carrying pigment of red blood cells. AIP results from partial deficiency of porphobilinogen deaminase (PBGD), an enzyme involved in the heme biosynthesis pathway. Symptoms occur due to the accumulation of porphyrin precursors, aminolevulinic acid (A... https://www.zupyak.com/p/4494525/t/the-acute-intermittent-porphyria-market-is-poised-to-witness-significant-growth-owing-to-increasing-disease-prevalence