Literature DB >> 27890718

Thalassaemia screening and confirmation of carriers in parents.

Angela N Barrett1, Ramasamy Saminathan2, Mahesh Choolani3.   

Abstract

Haemoglobinopathies are among the most common inherited monogenic disorders worldwide. Thalassaemia screening for carrier status is recommended for adults of reproductive age if suspected of being at risk. Conventional laboratory methods for screening include the assessment of haematological indices, and high-performance liquid chromatography, capillary electrophoresis or isoelectric focusing to measure the levels of HbA2 and HbF, and to identify haemoglobin variants. Each screening method has its advantages and disadvantages, the main disadvantage being that none can fully resolve all variants. The complex nature of the genetics of haemoglobinopathies necessitates expertise in the interpretation of screening results to evaluate the most likely genotypes, which must then be confirmed using the DNA diagnosis. This review highlights the limits and pitfalls of each screening technique, and outlines a rational combination of different methods to overcome issues in thalassaemia carrier detection.
Copyright © 2016. Published by Elsevier Ltd.

Entities:  

Keywords:  HbA2; carrier screening; haemoglobinopathy; red blood cell indices; thalassaemia trait

Mesh:

Substances:

Year:  2016        PMID: 27890718     DOI: 10.1016/j.bpobgyn.2016.10.015

Source DB:  PubMed          Journal:  Best Pract Res Clin Obstet Gynaecol        ISSN: 1521-6934            Impact factor:   5.237


  4 in total

1.  [Rapid detection of alpha-globin gene αααanti-3.7 triplets with droplet digital PCR].

Authors:  Xiao-Qian Gong; Xue-Huang Yang; Lin-Li Qiao; Ya-Jun Cheng; Wan-Jun Zhou
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2017-09-20

2.  Next Generation Sequencing in Newborn Screening in the United Kingdom National Health Service.

Authors:  Julia C van Campen; Elizabeth S A Sollars; Rebecca C Thomas; Clare M Bartlett; Antonio Milano; Matthew D Parker; Jennifer Dawe; Peter R Winship; Gerrard Peck; Darren Grafham; Richard J Kirk; James R Bonham; Anne C Goodeve; Ann Dalton
Journal:  Int J Neonatal Screen       Date:  2019-11-05

3.  Prenatal diagnosis of a rare β-thalassemia gene -90 (C>T) (HBB: c.-140 C>T) mutation associated with deletional Hb H disease (--SEA /-α4.2 ).

Authors:  Hou Qian; Jianlin Huang; Ji Xu; Weihua Zhao; Xiufeng Ye; Wenlan Liu
Journal:  Mol Genet Genomic Med       Date:  2020-09-03       Impact factor: 2.183

4.  Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population.

Authors:  Farjana Akther Noor; Nusrat Sultana; Golam Sarower Bhuyan; Md Tarikul Islam; Mohabbat Hossain; Suprovath Kumar Sarker; Khaleda Islam; Waqar Ahmed Khan; Mujahida Rahman; Syeda Kashfi Qadri; Hossain Uddin Shekhar; Firdausi Qadri; Syed Saleheen Qadri; Kaiissar Mannoor
Journal:  Orphanet J Rare Dis       Date:  2020-01-15       Impact factor: 4.123

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.