Literature DB >> 11113911

Accuracy of prenatal diagnosis for haemoglobin disorders in the UK: 25 years' experience.

J Old1, M Petrou, L Varnavides, M Layton, B Modell.   

Abstract

We have reviewed the accuracy of prenatal diagnosis for the thalassaemias and sickle cell disorders performed for UK residents since the service began in 1974. Prenatal diagnosis has been performed in 3254 pregnancies: 517 by fetal blood analysis, 681 by Southern blotting and 2056 by polymerase chain reaction (PCR) methods, the majority using the amplification refractory mutation system (ARMS). The number of homozygotes diagnosed was 808 (24.8%). Twenty-five diagnostic errors have been recorded, ten arising from non-laboratory errors (0.31%) and 15 due to technical problems associated with the diagnostic techniques. The latter group consisted of eight misdiagnoses by globin chain synthesis (1.55%), five by Southern blot analysis (0.73%) and two by PCR methods (0. 10%). The data show that the accuracy of prenatal diagnosis has improved with each development of diagnostic technique, and confirms that prenatal diagnosis of beta-thalassaemia and sickle cell disorders by ARMS-PCR is very accurate and reliable. The overall error rate for prenatal diagnosis by PCR methods in the UK is now 0. 41%. Copyright 2000 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11113911

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  8 in total

1.  Single tube genotyping of sickle cell anaemia using PCR-based SNP analysis.

Authors:  C M Waterfall; B D Cobb
Journal:  Nucleic Acids Res       Date:  2001-12-01       Impact factor: 16.971

2.  Molecular prenatal diagnosis of alpha and beta thalassemia in pregnant Hakka women in southern China.

Authors:  Pingsen Zhao; Heming Wu; Zhixiong Zhong; Liubing Lan; Mei Zeng; Hualan Lin; Huaxian Wang; Zhiyuan Zheng; Luxian Su; Wei Guo
Journal:  J Clin Lab Anal       Date:  2017-08-03       Impact factor: 2.352

3.  Prenatal diagnosis of sickle cell disease by the technique of PCR.

Authors:  Praneeta J Singh; A C Shrivastava; A V Shrikhande
Journal:  Indian J Hematol Blood Transfus       Date:  2014-07-08       Impact factor: 0.900

4.  Haematology in Africa.

Authors:  Lucio Luzzatto; Foluke Fasola; Léon Tshilolo
Journal:  Br J Haematol       Date:  2011-07-05       Impact factor: 6.998

5.  Molecular Genetic Characterization of β-Thalassemia and Sickle Cell Syndrome in the Albanian Population.

Authors:  A Babameto-Laku; A Mitre; S Berisha; V Mokini; D Roko
Journal:  Balkan J Med Genet       Date:  2011-06       Impact factor: 0.519

6.  Molecular analysis of hemoglobinopathies in a large ethnic Hakka population in southern China.

Authors:  Pingsen Zhao; Heming Wu; Ruiqiang Weng
Journal:  Medicine (Baltimore)       Date:  2018-11       Impact factor: 1.889

7.  EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.

Authors:  Joanne Traeger-Synodinos; Cornelis L Harteveld; John M Old; Mary Petrou; Renzo Galanello; Piero Giordano; Michael Angastioniotis; Barbara De la Salle; Shirley Henderson; Alison May
Journal:  Eur J Hum Genet       Date:  2014-07-23       Impact factor: 4.246

8.  Rapid detection of pathological mutations and deletions of the haemoglobin beta gene (HBB) by High Resolution Melting (HRM) analysis and Gene Ratio Analysis Copy Enumeration PCR (GRACE-PCR).

Authors:  Andrew Turner; Jurgen Sasse; Aniko Varadi
Journal:  BMC Med Genet       Date:  2016-10-19       Impact factor: 2.103

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.