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Early Physiotherapy Intervention of a Patient with Acute Intermittent Porphyria-A Single Case Study
2021
Indian Journal of Physiotherapy and Occupational Therapy
The Porphyrias are metabolic disorders, each resulting from the deficiency of a specific enzyme in the heme biosynthetic pathway. Acute intermittent porphyria (AIP) is an autosomal dominant inborn error characterized by decreased activity of porphobilinogen (PBG) deaminase leading to increased levels of haem precursors, namely amino levulinic acid (ALA) and PBG. The major manifestations of theacute hepatic porphyrias are neurologic-neuropathic abdominal pain, peripheral motor neuropathy, and
doi:10.37506/ijpot.v15i2.14508
fatcat:mwvi6i2u7jhl7ansrw4cdpy6l4