Literature DB >> 2064964

The spectrum of beta-thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis.

N Y Varawalla1, J M Old, R Sarkar, R Venkatesan, D J Weatherall.   

Abstract

The beta-thalassaemia mutations in 702 unrelated carriers originating from seven different regions of the Indian subcontinent have been characterized using allele specific priming of the polymerase chain reaction (PCR). It was possible to identify the mutations in 688 (98%) of the individuals studied. Eleven different mutations were identified, of which five common ones accounted for 93.6%; namely the ones at IVS-1 position 5 (G-C), codons 8/9 (+G), IVS-1 position 1 (G-T), codons 41/42 (-CTTT) and the 619 bp deletion at the 3' end of the gene. The mutations at IVS-2 position 1 (G-A) and codon 30 (G-C), previously undescribed in Asian Indians, were found in two and six individuals respectively. Some regional variation in the distribution of beta-thalassaemia alleles was noted. These findings should prove useful for the development of a first trimester prenatal diagnosis programme based on direct detection of mutations.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 2064964     DOI: 10.1111/j.1365-2141.1991.tb04423.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  42 in total

1.  Thalassaemia among Asians in Britain. Thalassaemia Society is working to improve awareness.

Authors:  N Lakhani
Journal:  BMJ       Date:  1999-03-27

2.  Prevention of thalassemia: a necessity in India.

Authors:  I C Verma; V P Choudhry; P K Jain
Journal:  Indian J Pediatr       Date:  1992 Nov-Dec       Impact factor: 1.967

3.  Analysis of beta-globin gene haplotypes in Asian Indians: origin and spread of beta-thalassaemia on the Indian subcontinent.

Authors:  N Y Varawalla; A C Fitches; J M Old
Journal:  Hum Genet       Date:  1992-12       Impact factor: 4.132

4.  A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka.

Authors:  M L Black; S Sinha; S Agarwal; R Colah; R Das; M Bellgard; A H Bittles
Journal:  J Community Genet       Date:  2010-10-10

5.  Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes.

Authors:  S Sinha; M L Black; S Agarwal; R Colah; R Das; K Ryan; M Bellgard; A H Bittles
Journal:  Hugo J       Date:  2010-02-10

Review 6.  Beta-thalassemias: expression, molecular mechanisms and mutations in Indians.

Authors:  R Colah; D Mohanty
Journal:  Indian J Pediatr       Date:  1998 Nov-Dec       Impact factor: 1.967

7.  Antenatal screening for identification of couples for prenatal diagnosis of severe hemoglobinopathies in surat, South gujarat.

Authors:  Dipal S Bhukhanvala; Smita M Sorathiya; Pratibha Sawant; Roshan Colah; Kanjaksha Ghosh; Snehalata C Gupte
Journal:  J Obstet Gynaecol India       Date:  2012-11-02

8.  Subclinical haemorrhagic tendency exists in patients with β-thalassaemia major in early childhood.

Authors:  Abhishek Maiti; Amartya Chakraborti; Puranjoy Chakraborty; Sanjay Mishra
Journal:  Australas Med J       Date:  2012-02-29

9.  Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction.

Authors:  Syahzuwan Hassan; Rahimah Ahmad; Zubaidah Zakaria; Zefarina Zulkafli; Wan Zaidah Abdullah
Journal:  Malays J Med Sci       Date:  2013-01

10.  Current Genetic Epidemiology of β-Thalassemias and Structural Hemoglobin Variants in the Lazio Region (Central Italy) Following Recent Migration Movements.

Authors:  Antonio Amato; Maria Pia Cappabianca; Alessia Colosimo; Maria Perri; Paola Grisanti; Ivo Zaghis; Donatella Ponzini; Maria Lerone
Journal:  Adv Hematol       Date:  2010-10-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.