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Case Reports
. 2019 Jul;70(1):434-436.
doi: 10.1002/hep.30543. Epub 2019 Jun 6.

Clinical Remission of Delta-Aminolevulinic Acid Dehydratase Deficiency Through Suppression of Erythroid Heme Synthesis

Rochus A Neeleman  1 , Eduard J van Beers  2 , Edith C Friesema  1 , Rita Koole-Lesuis  1 , Willem L van der Pol  3 , J H Paul Wilson  1 , Janneke G Langendonk  1
Affiliations
Case Reports

Clinical Remission of Delta-Aminolevulinic Acid Dehydratase Deficiency Through Suppression of Erythroid Heme Synthesis

Rochus A Neeleman et al. Hepatology. 2019 Jul.
No abstract available

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References

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    1. Thunell S, Henrichson A, Floderus Y, Groth CG, Eriksson B‐G, Barkholt L, et al. Liver transplantation in a boy with acute porphyria due to aminolaevulinate dehydratase deficiency. Eur J Clin Chem Clin Biochem 1992;30:599‐606. - PubMed
    1. Sassa S, Fujita H, Doss M, Hassoun A, Verstraeten L, Mercelis R, et al. Hereditary hepatic porphyria due to homozygous δ‐aminolevulinic acid dehydratase deficiency: studies in lymphocytes and erythrocytes. Eur J Clin Invest 1991;21:244‐248. - PubMed
    1. Gou E, Chan A, Penz C, Querbes W, Simon A, Anderson KE. 5‐Aminolevulinate dehydratase porphyria (ADP): evidence for hepatic ALAS1 induction. Poster and Oral Presentation, International Congress on Porphyrins and Porphyrias; June 27, 2017; Palais de la Bourse, Bordeaux, France.

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