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Double Heterozygous For Haemoglobin S and Haemoglobin E.

M M Rahman1, K Fatema, M M Hossain

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A rare double heterozygous state for hemoglobin S (HbS) and hemoglobin E (HbE) was identified in a Bangladeshi family. Documenting this uncommon genetic condition is crucial for family genetic counseling and reproductive risk assessment.

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Area of Science:

  • Hematology
  • Medical Genetics

Background:

  • Hemoglobin E (HbE) is prevalent in Bangladesh, while Hemoglobin S (HbS) is rare.
  • Co-inheritance of HbS and HbE is uncommon in the region, unlike HbE/β-thalassemia.

Observation:

  • A Bangladeshi family study identified two members with a double heterozygous state for HbS and HbE.
  • Other family members presented with single HbS or HbE gene inheritance.

Findings:

  • The study confirmed a rare double heterozygous state for HbS and HbE in a family.
  • This genetic condition, though uncommon, was documented in Dhaka, Bangladesh.

Implications:

  • Documentation of rare HbS/HbE double heterozygosity is vital for genetic counseling.
  • Understanding reproductive risks associated with this condition is important for affected families.