Evidence map›Paper›PMID 40687459›Full record

ArticleIndian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion2025

Mutation Analysis for Hemoglobinopathies in Eastern Jharkhand.

Shambhavi, Umesh Kumar Ojha, Mahino Fatima, Rani Manisha, Mohammed Faruq, Vivek Kumar

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Article in Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

ShambhaviDepartment of Pediatrics, Shaheed Nirmal Mahto Medical College , Dhanbad, Jharkhand India.ORCID 0000-0002-5580-2321
Umesh Kumar OjhaDepartment of Medicine, Shaheed Nirmal Mahto Medical College, Dhanbad, Jharkhand India.
Mahino FatimaDepartment of Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Rani ManishaDepartment of Medical Genetics, PostGraduate Institute of Child Health Noida, Noida, Uttar Pradesh India.
Mohammed FaruqDepartment of Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Vivek KumarDepartment of Medicine, Shaheed Nirmal Mahto Medical College, Dhanbad, Jharkhand India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thalassemia is the commonest monogenic disorder worldwide and India is home to significant proportion of these patients. The prevalence of beta-thalassemia trait varies around the country ranging from 0.35 to 37.5%. Data regarding mutation spectrum of beta thalassemia from Jharkhand are scanty, though this state has high prevalence of thalassemia. The Aim of study was to explore different mutations prevalent in transfusion-dependent-thalassemia patients in age group of 6 months to 18 years, coming to our centre over period of one month for regular transfusion. Basic characteristics were noted and blood sample were sent for genetic analysis. We studied 51 patients. Their mean age was 9 years. Severe β+/ severe β + was most common genotype found in 78.4% patients followed by severe β+/β0. We found that c.92 + 5 C > G was the commonest mutation. We also report one patient with extremely rare mutation called as Hb Monroe (c.92G > C). The mutation c.92 + 5 C > G has been reported as the commonest mutation in various regions of our country but its frequency varies from 55 to about 71.4%. We found even greater frequency of this mutation (88.2%) in our sample. This study serves to fill the gap in knowledge of mutation spectrum in this under-represented area of our country.

Indexed as

Hemoglobin monroeMutationThalassemia

Identifiers

PMID40687459
PMCPMC12267758

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