Homozygous Variegate Porphyria: Two Similar Cases in Unrelated Families
- 1 June 1986
- journal article
- case report
- Published by SAGE Publications in Journal of the Royal Society of Medicine
- Vol. 79 (6) , 361-363
- https://doi.org/10.1177/014107688607900614
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- Erythrocyte 5-Aminolaevulinic Acid Dehydrase Hydroxymethylbilane Synthase and Uroporphyrinogen Iii Synthase Activities in AlcoholicsClinical Science, 1984
- HOMOZYGOUS VARIEGATE PORPHYRIAThe Lancet, 1984
- Harderoporphyria: a variant hereditary coproporphyria.Journal of Clinical Investigation, 1983
- HEPATOERYTHROPOIETIC PORPHYRIA: A NEW UROPORPHYRINOGEN DECARBOXYLASE DEFECT OR HOMOZYGOUS PORPHYRIA CUTANEA TARDA?The Lancet, 1981
- A Plasma Porphyrin Fluorescence Marker for Variegate PorphyriaArchives of Dermatology, 1980
- The Enzymatic Defect in Variegate PorphyriaNew England Journal of Medicine, 1980