Hereditary Heinz-body Anaemia, Thrombocyttopenia, and Haemoglobinopathy (Hb Koln) in a Glasgow Family
- 31 October 1964
- Vol. 2 (5417) , 1099-1103
- https://doi.org/10.1136/bmj.2.5417.1099
Abstract
An abnormal hemo-globin (Hb Koln) has been observed in 10 members of a Glasgow family of remote German ancestry. Possession of this hemoglobin variant results in a form of hereditary Heinz-body anemia and thrombocytopenia. The clinical and laboratory findings in this family are presented and the characterization of the hemoglobin variant is described. The relationship of this variant to the hemolytic anemia, Heinz-body formation, and thrombocytopenia is discussed.Keywords
This publication has 22 references indexed in Scilit:
- Hereditary Heinz‐Body AnaemiaBritish Journal of Haematology, 1964
- HEMOLYTIC DISEASE ASSOCIATED WITH THE PRODUCTION OF ABNORMAL HEMOGLOBIN AND INTRAERYTHROCYTIC HEINZ BODIES.1963
- NOUVEAU CAS DANEMIE HEMOLYTIQUE CONGENITALE AVEC INCLUSIONS INTRA-ERYTHROCYTAIRES ET URINES NOIRES - IMPORTANCE DE LA SPLENECTOMIE DANS LAPPARITION DE CES INCLUSIONS1961
- ANEMIE HEMOLYTIQUE CONGENITALE AVEC INCLUSIONS INTRA-ERYTHROCYTAIRES ET URINES NOIRES - RAPPORT DUN NOUVEAU CAS AVEC ETUDE DE MICROSCOPIE ELECTRONIQUE1961
- Properties and Inheritance of Hæmoglobin by Asymmetric RecombinationNature, 1959
- TRIS Buffer for the Demonstration of Haemoglobin A2by Paper ElectrophoresisJournal of Clinical Pathology, 1959
- Starch Gel Electrophoresis in a Discontinuous System of BuffersNature, 1957
- A new technique for differentiation of hemoglobin.1957
- The Use of the Isotope 51Cr as a Label for Red CellsBritish Journal of Haematology, 1955
- Autohemolysis and Other Changes Resulting from the Incubation in Vitro of Red Cells from Patients with Congenital Hemolytic AnemiaBlood, 1954