Bone marrow delta-aminolaevulinate synthase deficiency in a female with congenital sideroblastic anemia.

Abstract:

:Heme biosynthesis was examined in erythroid tissue of a 4-yr-old girl with severe sideroblastic anemia since infancy, as documented by the presence of intramitochondrial deposits of iron in erythroblasts. Free red cell protoporphyrin, urinary porphyrins, and activities of erythrocyte porphobilinogen synthase, uroporphyrinogen 1 synthase, aspartate aminotransferase, and pyridoxine kinase were normal or increased. Bone marrow ferrochelatase activity was normal. Activity of bone marrow delta-aminolaevulinate (ALA) synthase was markedly reduced to 7 pmole ALA/10(6) erythroblasts/30 min (normal 127 +/- 29) but was enhanced fivefold by pyridoxal phosphate (normal 0%--25% increase). Therapy with oral pyridoxine and parenteral pyridoxal-5'-phosphate did not increase effective red cell production. The sideroblastic anemia in this patient appears to be related to a congenital defect in the initial step of heme biosynthesis.

journal_name

Blood

journal_title

Blood

authors

Buchanan GR,Bottomley SS,Nitschke R

subject

Has Abstract

pub_date

1980-01-01 00:00:00

pages

109-15

issue

1

eissn

0006-4971

issn

1528-0020

journal_volume

55

pub_type

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