Survival of two patients with severe delta-aminolaevulinic acid dehydratase deficiency porphyria
- PMID: 11286384
- DOI: 10.1023/a:1005610922789
Survival of two patients with severe delta-aminolaevulinic acid dehydratase deficiency porphyria
Abstract
The course of delta-aminolaevulinic acid dehydratase activity was studied over the 23 years in erythrocytes of two male patients. The enzyme activity was originally 1-2%, which then increased to approximately 8%, of normal levels several years after clinical manifestation of the acute hepatic porphyria syndrome. Urinary excretions of delta-aminolaevulinic acid and coproporphyrin III were excessively increased in the two patients with compound-heterozygous delta-aminolaevulinic acid dehydratase deficiency porphyria.
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