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July 27, 2025

Endocrine and metabolic manifestations of thalassemia in Bangladeshi patients: A narrative review

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Authors

AMAbdullah Al MosabbirMMMd Shahed Morshed

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Overview

Narrative review summarizes endocrine and metabolic complications in thalassemia patients in Bangladesh, suggesting urgent interdisciplinary collaboration.

Key Points

  • Thalassemia leads to endocrine and metabolic complications due to hormone deficiencies from iron deposition.
  • Evidence regarding glycemic, adrenal, and pituitary status in these patients remains scarce.
  • Collaboration among endocrinologists, hematologists, and transfusion specialists is essential for improved outcomes.
  • Increased life expectancy highlights the need for effective management of complications from thalassemia.

Cite This Study

Mosabbir et al. (2025) studied this question.

synapsesocial.com/papers/689a0939e6551bb0af8ce75dhttps://doi.org/10.3329/jacedb.v2i1.78432
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Endocrinopathies in Thalassemia – A Hospital-based Study in Bangladesh2024
  2. 2Endocrine Manifestations in Children and Adolescents with Thalassemia Major - A Prospective Cohort Study2025
  3. 3Endocrine dysfunctions in patients with beta thalassemia major: a single-center retrospective study from Basrah2026
  4. 4Endocrinopathies in adult Egyptian thalassemia patients, a cross-section study, single-center experience2025
  5. 5Bone Mineral Density and Endocrinopathies in Adults with Transfusion-Dependent Beta-Thalassemia Major Patients from Oman2024