Literature DB >> 4753245

Screening for abnormal haemoglobins: a pilot study.

J Stuart, F C Schwartz, A J Little, D N Raine.   

Abstract

A pilot study has been made of the implication of screening for abnormal haemoglobins in immigrant schoolchildren. An abnormality was detected by capillary blood haemoglobin electrophoresis in 8.4% of 6,835 children and a haemoglobinopathy outpatient clinic had to be established to deal with the heavy work load which resulted. The clinic was also used to determine the value of investigating the remaining members of the family once an abnormality had been detected in one child.Healthy siblings with normal haemoglobin electrophoretic patterns and normal iron and folate levels were studied to determine a normal range for haemoglobin in relation to age for adequately nourished immigrant children. The lower limit of the normal range was close to the mean value minus 1(1/2) S.D.; by using this definition 10.3% of 280 children were subsequently found to be anaemic.Population screening of this type is desirable, but further pilot studies of patient education, genetic counselling, organization of specimen collection, data processing, and follow-up health care facilities are required before screening is extended more widely in the United Kingdom.

Entities:  

Mesh:

Substances:

Year:  1973        PMID: 4753245      PMCID: PMC1587332          DOI: 10.1136/bmj.4.5887.284

Source DB:  PubMed          Journal:  Br Med J        ISSN: 0007-1447


  14 in total

1.  NORMAL RED BLOOD PICTURE DURING THE FIRST THREE YEARS OF LIFE.

Authors:  P J MOE
Journal:  Acta Paediatr Scand       Date:  1965-01

Review 2.  HUMAN HAEMOGLOBINS.

Authors:  E R HUEHNS; E M SHOOTER
Journal:  J Med Genet       Date:  1965-03       Impact factor: 6.318

3.  Rapid celluose acetate electrophoresis. II. Qualitative and quantitative hemoglobin fractionation.

Authors:  R C BARTLETT
Journal:  Clin Chem       Date:  1963-06       Impact factor: 8.327

4.  A new technique for differentiation of hemoglobin.

Authors:  A R ROBINSON; M ROBSON; A P HARRISON; W W ZUELZER
Journal:  J Lab Clin Med       Date:  1957-11

5.  Sickle cell anemia: national program raises problems as well as hopes.

Authors:  B J Culliton
Journal:  Science       Date:  1972-10-20       Impact factor: 47.728

6.  Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Authors:  K SINGER; A I CHERNOFF; L SINGER
Journal:  Blood       Date:  1951-05       Impact factor: 22.113

7.  Why do sickle screening in children?

Authors:  N Fost; N M Kaback
Journal:  Pediatrics       Date:  1973-04       Impact factor: 7.124

8.  Sickle cell disease.

Authors:  H M Ranney
Journal:  Blood       Date:  1972-03       Impact factor: 22.113

9.  Normal haematological values in the Central American population.

Authors:  F E Viteri; V De Tuna; M A Guzmán
Journal:  Br J Haematol       Date:  1972-08       Impact factor: 6.998

10.  Red cell lifespan in hemoglobin C disorders (with special reference to hemoglobin C trait).

Authors:  K H Prindle; P R McCurdy
Journal:  Blood       Date:  1970-07       Impact factor: 22.113

View more
  11 in total

1.  Neonatal screening for haemoglobinopathy. Results in 7691 Manchester newborns.

Authors:  D I Evans; V M Blair
Journal:  Arch Dis Child       Date:  1976-02       Impact factor: 3.791

2.  Services for sickle cell disease: unified approach needed.

Authors:  I M Franklin
Journal:  Br Med J (Clin Res Ed)       Date:  1988-02-27

Review 3.  Haemoglobin D Punjab (D Los Angeles).

Authors:  F Vella; H Lehmann
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

4.  Editorial: Screening for sickle-cell disease.

Authors: 
Journal:  Br Med J       Date:  1974-09-21

5.  Tropical conditions with special reference to an immigrant population. Haemoglobinopathies.

Authors:  D J Stoker
Journal:  Proc R Soc Med       Date:  1974-09

6.  Poor prognosis of acute lymphoblastic leukaemia in Asian children living in the United Kingdom.

Authors:  A Oakhill; J R Mann
Journal:  Br Med J (Clin Res Ed)       Date:  1983-03-12

7.  Screening and counselling of school-leavers for the carrier state of hereditary anaemias.

Authors:  E Lobo; D S Thompson
Journal:  Br Med J (Clin Res Ed)       Date:  1982-05-01

8.  Management of sickle-cell disease.

Authors:  J Stuart
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

9.  Sickle cell haemoglobinopathies in England.

Authors:  J R Mann
Journal:  Arch Dis Child       Date:  1981-09       Impact factor: 3.791

10.  Neonatal screening for sickle haemoglobinopathies in Birmingham.

Authors:  K D Griffiths; D N Raine; J R Mann
Journal:  Br Med J (Clin Res Ed)       Date:  1982-03-27
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.