Mutation Spectrum of β-Thalassemia and Other Hemoglobinopathies in Chittagong, Southeast Bangladesh. (2nd November 2015)
- Record Type:
- Journal Article
- Title:
- Mutation Spectrum of β-Thalassemia and Other Hemoglobinopathies in Chittagong, Southeast Bangladesh. (2nd November 2015)
- Main Title:
- Mutation Spectrum of β-Thalassemia and Other Hemoglobinopathies in Chittagong, Southeast Bangladesh
- Authors:
- Chatterjee, Tridip
Chakravarty, Amit
Chakravarty, Sudipa
Chowdhury, Mahmood Ahmed
Sultana, Razia - Abstract:
- Abstract: Thalassemia is one of the most common autosomal recessive blood disorders in the world. It shows a variety of clinical expression, starting from asymptomatic to severe blood transfusion dependence. More than 500 alleles have been characterized in or around the β-globin region. Moreover, most geographical regions have their own characteristics, frequency and availability of these alleles, predominantly circulating within the communities present in that particular region. In this study, we explored the spectrum of β-thalassemia (β-thal) alleles present in Chittagong, Southeast Bangladesh. This study comprises β-thal and Hb E ( HBB : c.79 G > A) patients from in and around the area of Chittagong. Not only exploring the complete β-globin mutation spectrum of the area, but we also tried to look at the origin of the mutated alleles. The β-thal mutations of Bangladesh show a relatively wide spectrum of alleles, which further demonstrates the heterogeneity of the disease in this country. Although our study showed that the majority of the mutations have their origin in neighboring countries such as India, countries of Southeast Asia, Pakistan, etc., some unusual alleles do not originate in neighboring countries and put a little more diversity in the overall spectrum of β-thal-specific alleles. Overall, this study demonstrates the mutation spectrum related to β-thal in Chittagong, Southeast Bangladesh.
- Is Part Of:
- Hemoglobin. Volume 39:Number 6(2015)
- Journal:
- Hemoglobin
- Issue:
- Volume 39:Number 6(2015)
- Issue Display:
- Volume 39, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 39
- Issue:
- 6
- Issue Sort Value:
- 2015-0039-0006-0000
- Page Start:
- 389
- Page End:
- 392
- Publication Date:
- 2015-11-02
- Subjects:
- Amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) -- β-globin mutations, -- β-thalassemia (β-thal) -- Hb A2/E -- Hb E-β-thalassemia (Hb E-β-thal) -- mean corpuscular volume (MCV) -- mean corpuscular hemoglobin (MCH)
Hemoglobinopathy -- Periodicals
Hemoglobin -- Periodicals
Hematology -- Periodicals
Thalassemia -- Periodicals
Blood -- Diseases -- Periodicals
612.1111 - Journal URLs:
- http://informahealthcare.com/journal/hem ↗
http://informahealthcare.com ↗ - DOI:
- 10.3109/03630269.2015.1078810 ↗
- Languages:
- English
- ISSNs:
- 0363-0269
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.040000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11389.xml