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Browsing PhD Thesis by Issue Date

Browsing PhD Thesis by Issue Date

Now showing items 1-6 of 6

Genetic diversity among Bangali and seven ethnic groups of Bangladesh based on Y-chromosome

Hasan, Md. Mahamud (University of Dhaka, 2021-08-24)

A comprehensive population genetic study was conducted using 17 Y-chromosome specific microsatellites to decipher genetic diversity of the Bangladeshi populations from a Y-chromosome perspective. Seven ethnic populations ...
Genetic Spectrum and Metabolic Profiling of Congenital Hypothyroid Children in Hospital Care Settings in Bangladesh

Begum, Mst. Noorjahan (University of Dhaka, 2021-08-26)

Congenital Hypothyroidism (CH) is the deficiency of thyroid hormones at birth and a major cause of mental retardation if left untreated. The frequency of CH is much higher in Bangladesh than that of the global incidences ...
Inborn errors of metabolism screening and profiling of amino acids, acylcarnitines and glucose-6-phosphate dehydrogenase deficiency in Bangladesh population

Sarker, Suprovath Kumar (University of Dhaka, 2021-08-29)

Similar to other lower and lower middle income countries, Bangladesh is facing the accelerated demographic shift from communicable diseases to non-communicable diseases (NCDs) including genetic disorders (GDs). Approximately ...
Metabolomics Profiling for Amino Acidopathies of Infants in Hospital Based Settings in Bangladesh and Development of Easy-to-Use Kit for Disease Diagnosis and Monitoring

Hossain, Md. Shawkat (©University of Dhaka, 2025-02-09)

This study aimed to address the challenges associated with identifying inborn errors of metabolism (IEM) in resource-constrained environments, focusing on amino acid and galactose metabolism disorders in the Bangladeshi ...
Impacts of pathogenic mutations and XmnI polymorphism on the severity of haemoglobin E β-thalassaemia patients in Bangladesh

Aziz, Md. Abdul (© University of Dhaka, 2025-07-07)

Background: Haemoglobin E β-thalassaemia is a common blood disorder in South Asia, especially Bangladesh. The disorder can range from mild and asymptomatic anemia to life-threatening anemia. Patients with asymptomatic ...
Molecular Basis of the Pelvi-Ureteric Junction Obstruction in Children with Hydronephrosis

SHADRUL ALAM, MOHAMMED (© University of Dhaka, 2025-11-05)

ABSTRACT: Background: Pelvi-Ureteric Junction Obstruction (PUJO) represents a significant cause of congenital hydronephrosis that can lead to progressive renal damage if untreated. While the condition is well-characterized ...

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