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Open access Oct 2026

Transfusion, and reproductive health profiles of female patients with transfusion-dependent thalassaemia in Bangladesh: A cross-sectional study

Background: Regular iron chelation therapy is critical to prevent iron overload complications in transfusion-dependent patients. However, adherence remains suboptimal, thalassaemia is one of the most common inherited hemoglobin disorders worldwide, with a particularly high burden in South and Southeast Asia. Objectives...

Mehnaj Ashraf, S. Selim, Md. Salahuddin Shah et al. · 0 citations
Open access Oct 2026

An unusually severe hemorrhagic phenotype leading to prolonged diagnostic delay in PTPN11 variant Noonan syndrome

Background: Noonan syndrome is a RASopathy which carries autosomal dominant inheritance and is characterized by variable phenotypic expression involving craniofacial, cardiovascular, skeletal, hematological, and neurodevelopmental abnormalities. Bleeding manifestations are common and may result from platelet dysfunctio...

Tasnim Nusrat, Md. Latiful Bari, S. Selim et al. · 0 citations

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