Hereditary Haemolytic Anaemia due to an Abnormal Haemoglobin (Haemoglobin Kings County)
- 1 December 1968
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 15 (6) , 579-588
- https://doi.org/10.1111/j.1365-2141.1968.tb01580.x
Abstract
Two patients in an American Negro family with a hereditary non‐spherocytic haemolytic Heinz‐body anaemia, mesobilifuscinuria, and an abnormal haemoglobin have been studied. The absence of any abnormality in the red cell metabolism and the presence of a thermolabile fraction of the haemoglobin constituting 10 per cent of the patients’total haemoglobin make us believe that the cause of the haemolysis is the abnormal haemoglobin. Since this haemoglobin appears to differ from all the other abnormal haemoglobins described in patients having congenital non‐spherocytic haemolytic anaemia, a new name (haemoglobin Kings County) is proposed for it.Keywords
This publication has 22 references indexed in Scilit:
- Haemoglobin Hammersmith (β 42 (CD1) Phe→Ser)Nature, 1967
- Haemoglobin Sydney: β67 (EII) Valine→ Alanine : an Emerging Pattern of Unstable HaemoglobinsNature, 1967
- Haemoglobin Genova: β28 (B10) Leucine→ProlineNature, 1967
- Haemoglobin Köln (β–98 Valine → Methionine): An Unstable Protein Causing Inclusion-Body AnaemiaNature, 1966
- Hemoglobin Zürich: Clinical, chemical and kinetic studiesThe American Journal of Medicine, 1965
- Determination of oxygen equilibria with a versatile new tonometerAnalytical Biochemistry, 1965
- Human HaemoglobinsJournal of Medical Genetics, 1965
- Hereditary Heinz‐Body AnaemiaBritish Journal of Haematology, 1964
- Congenital Heinz‐Body AnaemiaBritish Journal of Haematology, 1964
- Une micro-méthode de l’immuno-électrophorèseInternational Archives of Allergy and Immunology, 1955