Acute Intermittent Porphyria
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Acute intermittent porphyria (AIP) is a rare autosomal dominant metabolic disorder affecting the production of heme, the oxygen-binding prosthetic group of hemoglobin. It is characterized by a deficiency of the enzyme porphobilinogen deaminase.
This video in 30 seconds
This video covers acute intermittent porphyria (AIP), a rare autosomal dominant metabolic disorder affecting the production of heme, the oxygen-binding prosthetic group of hemoglobin. It explains that AIP is characterized by a deficiency of the enzyme porphobilinogen deaminase.
Key points
- Defines AIP as a rare autosomal dominant metabolic disorder
- Covers its effect on production of heme
- Identifies porphobilinogen deaminase deficiency as its characteristic feature
Video Overview
This video presents “Acute Intermittent Porphyria” — Acute intermittent porphyria (AIP) is a rare autosomal dominant metabolic disorder affecting the production of heme, the oxygen-binding prosthetic group of hemoglobin. It is characterized by a deficiency of the enzyme porphobilinogen. Whether you are preparing for a procedure, studying the technique, or learning how a condition is assessed, the recording shows the process as it is performed in practice.
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