A5048095095- Iron Metabolism and Disorders
- Hemoglobinopathies and Related Disorders
- Hematological disorders and diagnostics
- Bone and Joint Diseases
- HIV-related health complications and treatments
- Acute Lymphoblastic Leukemia research
- Peripheral Nerve Disorders
- Orthopedic Surgery and Rehabilitation
- Orthopedic Infections and Treatments
- Digital Imaging for Blood Diseases
- Acute Myeloid Leukemia Research
- Prenatal Screening and Diagnostics
- COVID-19 Impact on Reproduction
Bangabandhu Sheikh Mujib Medical University
2017-2025
Background: Dengue fever, a major public health challenge in tropical regions, shows increasing incidence and severity worldwide, with frequent outbreaks Bangladesh. Vitamin D, known for its immune-modulating properties, has been suggested to influence outcomes viral infections, including dengue. This study aimed evaluate the vitamin D status among dengue patients examine association disease recovery outcomes. Methods: hospital-based cross-sectional was conducted from January 2022 December...
Introduction: Thalassemia, a hereditary hemoglobinopathy, causes chronic hemolytic anemia and complications like hypogonadism due to iron overload endocrine dysfunction. Despite advancements in transfusion chelation therapies, gonadal dysfunction remains prevalent. This study aims assess function beta-thalassemia patients, exploring hormonal profiles, pubertal development, menstrual irregularities improve disease management quality of life affected individuals. Objectives: To its association...
Background: The WHO estimates that about 7% of the world population are thalassaemia trait and increasing number cases being detected. carrier b thalassamia is reported to be more than 100 million. Bangladesh also lies in thalassaemic Belt. A conservative health report 3% our populations which means there 3-6 million Bangladesh. To manage trait, traditional concept not give iron or conaining food. But concomitant deficiency anaemia patient may fatal. Those patients should evaluated by serum...
Background: Acute leukaemia (AL) are a heterogenous group of haematological malignancy characterized by uncontrolled clonal proliferation haematopoietic progenitor cells. Objectives: The study was conducted to have detailed understanding immunophenotyping profile, the frequency discrepancy between bone marrow morphology and importance in diagnosis acute leukaemia. Methods: This prospective type observational carried out with an aim correlate immunophenotype bone
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Background: Carpal Tunnel Syndrome (CTS) is a constellation of symptoms and signs caused by entrapment the median nerve at wrist. Nerve Conduction Study (NCS) serve as an objective supplementary modality in diagnosis CTS used for severity assessment with high degree sensitivity specificity. Severity crucial step defining prognosis CTS. Methodology: The study was hospital based observational cross sectional conducted department Neurology, DMCH on 50 patients clinical electro-physiological...
Here we describe a case of 20-year-old, otherwise healthy man, who consulted physician due to acute low back pain presenting for couple days. Pain appeared suddenly, without any preceding trauma. Physical examination was unremarkable. Initial laboratory tests showed elevated inflammatory marker and thrombocytopenia. Patient treated conservatively but increasing MRI spine with contrast advised which feature suggestive infiltrative disease. Eventually patient diagnosed as lymphoblastic...
Beta thalassaemia is one of the most prevalent haemolytic disorders worldwide which poses serious economic burden to society. Study on clinical and demographic pattern this disorder will help concern authorities figure out problem. This cross-sectional descriptive study was carried determine socio-demographic characteristics as well find existence other co-morbidities among ?-thalassaemic patients (n-101). The at Department Haematology, Bangabandhu Sheikh Mujib Medical University (BSMMU)...
Background: Aberrant expression (AE) of Acute Leukaemia (AL) is essential to confirm the diagnosis AL patients whether it biphenotypic/mix phenotypic or with AE. Objectives: This study conducted observe diversity aberrant immunophenotypic expressions among acute leukaemia varying frequencies, find out correlation between aberrantly expressed markers different variety French American British (FAB) sub classification and any clinical presentation markers. Methodology: cross-sectional...
Background: Hb-E/Beta thalassaemia is a congenital haemoglobin disorder which compound heterozygous state consists of qualitative like Hb E variant & quantitative caused by genetic mutation Beta chain. Objective: The aim the study was to identify beta gene in E/Beta thalassaemia. Method: A total 32 diagnosed patients were included this cross-sectional from May 2019 July 2020. Genetic analysis done sanger sequencing. Results: In observational study, we found 13 different types mutations....