Coexistence of hereditary coproporphyria and porphyria cutanea tarda: A new type of a dual porphyria;Koexistenz von hereditärer koproporphyrie und porphyria cutanea tarda: Eine neue form einer dualen porphyrie

Medizinische Klinik

Volumn 97, Issue 1, 2002, Pages 1-5

  Doss, Manfred O ^a   Groß, Ulrich ^a   Puy, Hervé ^b   Doss, Margareta ^a   Kühnel, Alexandra ^a   Jacob, Karl ^c   Deybach, Jean Charles ^b   Nordmann, Yves ^b  

^a UNIVERSITY HOSPITAL MARBURG   (Germany)

^b HÔPITAL LOUIS MOURIER   (France)

^c LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

Author keywords

Coproporphyrinogen oxidase; Decarboxylase; Dual porphyrias; Hereditary coproporphyria; Mutation; Porphyria cutanea tarda; Uroporphyrinogen

Indexed keywords

COPROPORPHYRIN; PORPHYRINOGEN; UROPORPHYRINOGEN DECARBOXYLASE;

ADULT; ARTICLE; CASE REPORT; DENATURING GRADIENT GEL ELECTROPHORESIS; ERYTHROCYTE; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; HORMONAL REGULATION; HUMAN; POINT MUTATION; PORPHYRIA CUTANEA TARDA; PORPHYRIN METABOLISM; STEM CELL;

ADULT; COPROPORPHYRINOGEN OXIDASE; FEMALE; HETEROZYGOTE DETECTION; HUMANS; POINT MUTATION; PORPHYRIA CUTANEA TARDA; PORPHYRIAS, HEPATIC; UROPORPHYRINOGEN DECARBOXYLASE;

EID: 18244362109     PISSN: 07235003     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00063-002-1117-0     Document Type: Article

References (22)

1. Disorders of heme biosynthesis: X-linked sideroblastic anemia and the porphyrias
2. Coexistent variegate porphyria and porphyria cutanea tarda
3. Porphyrins and porphyrin precursors
4. New dual form of porphyria
5. Dual porphyria in double heterozygotes with porphobilinogen deaminase and uroporphyrinogen decarboxylase deficiencies
6. The porphyrias
7. Arzneistoffe bei akuten hepatischen porphyrien und empfehlungen zur anästhesic
8. Alcohol-induced decrease in uroporphyrinogen decarboxylase activity in rat liver and spleen
9. Hereditäre koproporphyrie in der bundesrepublik Deutschland
10. Porphyria cutanea tarda
11. Coexistence of deficiencies of uroporphyrinogen III synthase and decarboxylase in a patient with congenital erythropoietic porphyria and his family
12. Erythropoietic and hepatic porphyrias
13. Accurate and specific HPLC assay of coproporphyrinogen oxidase activity in human peripheral leucocytes
14. Porphyria cutanea tarda (chronische hepatische porphyrie)
15. Hereditary coproporphyria in Germany: Clinical-biochemical studies in 53 patients
16. Chester porphyria
17. Coexistent hereditary coproporphyria and congenital erythropoietic porphyria (Günther disease)
18. Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update
19. Dual porphyria of coexisting variegata and cutanea tarda
20. Hereditary uroporphyrinogen-decarboxylase-deficiency predisposing porphyria cutanea tarda (chronic hepatic porphyria) in females after oral contraceptive medication
21. Uroporphyrinogen decarboxylase and protoporphyrinogen oxidase in dual porphyria
22. Porphyria variegata and porphyria cutanea tarda in siblings: Chemical and genetic aspects