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Congenital erythropoietic porphyria, diminished activity of uroporphyrinogen decarboxylase and dyserythropoiesis.

AuthorsJ P Kushner, N R Pimstone, C R Kjeldsberg, M A Pryor, A Huntley
JournalBlood (Blood) Vol. 59 Issue 4 Pg. 725-37 (Apr 1982) ISSN: 0006-4971 [Print] United States
PMID7059676 (Publication Type: Case Reports, Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Porphyrins
  • Hydroxymethylbilane Synthase
  • Carboxy-Lyases
  • Uroporphyrinogen Decarboxylase
  • Uroporphyrinogen III Synthetase
Topics
  • Bone Marrow (ultrastructure)
  • Carboxy-Lyases (deficiency)
  • Erythrocytes (pathology)
  • Erythrocytes, Abnormal (pathology)
  • Erythropoiesis
  • Feces (analysis)
  • Humans
  • Hydroxymethylbilane Synthase (blood)
  • Male
  • Middle Aged
  • Pedigree
  • Porphyrias (blood, congenital, enzymology)
  • Porphyrins (blood, urine)
  • Skin Diseases (blood, congenital, enzymology)
  • Uroporphyrinogen Decarboxylase (blood, deficiency)
  • Uroporphyrinogen III Synthetase (blood)

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