Hereditary Hypochromic Anemia with Transfusion Hemosiderosis Treated with Pyridoxine
- 3 September 1959
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 261 (10) , 486-489
- https://doi.org/10.1056/nejm195909032611004
Abstract
ALTHOUGH pyridoxal-5-phosphate is known to serve as a coenzyme in the synthesis of heme,1 anemia associated with pyridoxine deficiency has been reported only rarely in human beings. Snyderman and her co-workers2 described an increase in reticulocytes and hemoglobin concentration in an infant treated with vitamin B6 who had become anemic while receiving a pyridoxine-deficient diet. More recently Harris and his co-workers3 reported a therapeutic response to pyridoxine in an anemic adult male. This patient was vitamin B6 deficient as evidenced by abnormalities of tryptophane metabolism. Since the report of Harris et al. several other patients have been described . . .Keywords
This publication has 6 references indexed in Scilit:
- Evidence for the Involvement of Ferrous Iron in the Biosynthesis of δ-Aminolævulic Acid by Chicken Erythrocyte PreparationsNature, 1958
- Metal Chelates of Pyridoxylidene Amino AcidsJournal of the American Chemical Society, 1957
- Pyridoxine Responsive Anemia in the Human Adult.Experimental Biology and Medicine, 1956
- IDIOPATHIC HEMOCHROMATOSIS, AN IRON STORAGE DISEASEMedicine, 1955
- PYRIDOXINE DEFICIENCY in the HUMAN INFANTThe American Journal of Clinical Nutrition, 1953
- HEREDITARY (?SEX-LINKED) ANEMIAThe Lancet Healthy Longevity, 1946