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Detection of Residual Donor Erythroid Progenitor Cells after Hematopoietic Stem Cell Transplantation for Patients with Hemoglobinopathies
Published on: September 6, 2017
[Alpha-thalassemia with Hb G-Philadelphia incidentally discovered during HbA1c testing]
Sophia Kahouli1, Azlarab Masrar2, Souad Benkirane2
1Laboratoire de Recherche et d'Analyses Médicales de la Gendarmerie Royale, Laboratoire d'Hématologie de l'Hôpital Militaire d'Instruction Mohammed V, Faculté de Médecine et de Pharmacie, Université Mohammed V, Rabat.
Annales De Biologie Clinique
|July 18, 2026
Summary
Hemoglobin G-Philadelphia, an alpha-globin variant, can cause anemia when homozygous or with alpha-thalassemia. This case highlights challenges in diagnosing this rare hemoglobinopathy.
Area of Science:
- Hematology
- Genetics
- Clinical Diagnostics
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