Hemoglobin Beth Israel
- 15 July 1976
- journal article
- case report
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 295 (3), 125-130
- https://doi.org/10.1056/nejm197607152950302
Abstract
We found that an abnormal hemoglobin with a very low oxygen affinity was responsible for overt cyanosis in an otherwise healthy adolescent. Hemoglobin Beth Israel, in which serine replaces the asparagine residue normally present at position 102 (G4) of the βpolypeptide chain, was associated with normal blood counts and no apparent exercise intolerance in the heterozygous carrier. Cyanosis resulted from a drastically right-shifted oxygen dissociation curve, whose position and shape could account for the absence of "physiologic" anemia. The whole-blood oxygen tension at 50 per cent oxygen saturation was 88 mm Hg (normally 26 ± 1 mm Hg), and the arterial blood was only 63 per cent saturated with oxygen despite a normal oxygen tension of 97 mm Hg. The hemolysate showed a low oxygen affinity but normal Bohr effect. Unexplained cyanosis, particularly in association with normal arterial oxygen tension should prompt a search for an abnormal hemoglobin, which may obviate the need for invasive diagnostic procedures. (N Engl J Med 295:125–130, 1976)Keywords
This publication has 24 references indexed in Scilit:
- Haemoglobin titusville: α94 Asp → AsnBiochimica et Biophysica Acta (BBA) - Protein Structure, 1975
- Structures of deoxy and carbonmonoxy haemoglobin Kansas in the deoxy quaternary conformationJournal of Molecular Biology, 1975
- Stereochemistry of Cooperative Effects in HemoglobinCold Spring Harbor Symposia on Quantitative Biology, 1972
- Studies on the function of abnormal hemoglobins II. Oxygen equilibrium of abnormal hemoglobins: Shimonoseki, Ube II, Hikari, Gifu, and AgenogiBiochimica et Biophysica Acta (BBA) - Protein Structure, 1970
- Hemoglobin Yoshizuka (G10(108)β asparagine→aspartic acid): a new variant with a reduced oxygen affinity from a Japanese familyJournal of Clinical Investigation, 1969
- Erythrocytosis associated with hemoglobin Rainier: oxygen equilibria and marrow regulationJournal of Clinical Investigation, 1969
- Abnormal human haemoglobins: Separation and characterization of the α and β chains by chromatography, and the determination of two new variants, Hb chesapeake and Hb J (Bangkok)Journal of Molecular Biology, 1966
- A HUMAN HEMOGLOBIN WITH LOWERED OXYGEN AFFINITY AND IMPAIRED HEME-HEME INTERACTIONS*Journal of Clinical Investigation, 1961
- Observations on the Minor Basic Hemoglobin Component in the Blood of Normal Individuals and Patients with ThalassemiaJournal of Clinical Investigation, 1957
- PROTEIN COAGULATION AND ITS REVERSALThe Journal of general physiology, 1930