Document Detail


Thalassaemia in the British.
MedLine Citation:
PMID:  4124395     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Different forms of thalassaemia or related disorders were found in 116 people of apparently pure British stock. Among them were one family with a child homozygous for beta-thalassaemia and eight heterozygous relatives, 16 families with 83 persons heterozygous for beta-thalassaemia, two families with three persons with Hb H disease and three heterozygous for alpha-thalassaemia 1, one family with a child apparently homozygous for the "silent beta-thalassaemia gene," one family with six members heterozygous for a form of beta-thalassaemia intermedia, and three families with 11 members heterozygous for different types of hereditary persistence of fetal haemoglobin. The clinical, haematological, and haemoglobin biosynthetic findings in these persons were similar to those of patients with thalassaemia from other racial groups. The heterozygous state for beta-thalassaemia is overlooked in British patients, particularly during pregnancy, because it is not considered in the differential diagnosis of refractory anaemia. In many cases this leads to much unnecessary investigation and potentially harmful treatment.There seem to be several varieties of hereditary persistence of fetal haemoglobin production among British people. These conditions, while not causing anaemia, may cause difficulties during examination of maternal blood for fetal cells and may, if inherited with a beta-thalassaemia gene, produce an unusually high level of Hb F in a person heterozygous for beta-thalassaemia.
Authors:
H H Knox-Macaulay; D J Weatherall; J B Clegg; M E Pembrey
Related Documents :
4124395 - Thalassaemia in the british.
24571145 - Stonewall list shows increased diversity in nhs workplaces.
16402095 - Acetylcholine.
21678215 - Is continuous sedation at the end of life an ethically preferable alternative to physic...
22606995 - The four principles: can they be measured and do they predict ethical decision making?
12405465 - Ethical dilemmas confronting dentists in queensland, australia.
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  British medical journal     Volume:  3     ISSN:  0007-1447     ISO Abbreviation:  Br Med J     Publication Date:  1973 Jul 
Date Detail:
Created Date:  1973-10-02     Completed Date:  1973-10-02     Revised Date:  2010-10-26    
Medline Journal Info:
Nlm Unique ID:  0372673     Medline TA:  Br Med J     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  150-5     Citation Subset:  AIM; IM    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adolescent
Anemia / diagnosis
Beta-Globulins
Carbon Isotopes
Diagnosis, Differential
Female
Fetal Hemoglobin
Great Britain
Hemoglobin H
Hemoglobinopathies / epidemiology
Humans
Leucine / metabolism
Male
Thalassemia / diagnosis,  epidemiology*,  genetics
Chemical
Reg. No./Substance:
0/Beta-Globulins; 0/Carbon Isotopes; 61-90-5/Leucine; 9034-63-3/Fetal Hemoglobin; 9034-79-1/Hemoglobin H
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Specificity of antibodies in amphibian larvae possessing a small number of lymphocytes.
Next Document:  Lead pollution: records in Southern California coastal sediments.