ORPHA:79276
Acute intermittent porphyria
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Adolescent, Adult
- Estimated prevalence
- <1 / 1 000 000 (Europe)
- Rarity class
- <1 / 1 000 000
ORPHA:79276 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.
Common signs
- Abdominal pain
- Elevated urinary delta-aminolevulinic acid
- Porphyrinuria
- Increased urinary porphobilinogen
- Abnormal enzyme/coenzyme activity
- Renal insufficiency