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Hypertension and renal disease in patients with acute intermittent porphyria

✍ Scribed by Dr. C. ANDERSSON; F. LITHNER


Book ID
114742764
Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
574 KB
Volume
236
Category
Article
ISSN
0954-6820

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Diminished activity of uroporphyrinogen I-synthetase in the liver and other tissues may be regarded to be the primary genetic deficiency of acute intermittent porphyria (AIP). Increased production and renal excretion of delta-aminolevulinic acid (ALA) und porphobilinogen (PBG) are secondary phenomen