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Report of Three Bengali Cases with Hemoglobin E Variant in Najran

مؤلف البحث
Mohamed Samir M. Khalil, Awad M. Al Qahtani, Jobran M. AlQahtani, Mohamed Mahmoud El Khawanky
مجلة البحث
Journal of Applied Hematology.
Accepted: 18 Sep 2020
المشارك في البحث
الناشر
NULL
تصنيف البحث
1
عدد البحث
NULL
موقع البحث
NULL
سنة البحث
2020
صفحات البحث
NULL
ملخص البحث

Abstract:
INTRODUCTION: Differential diagnosis of hemoglobin (Hb) variants eluting in the A2 window on
high‑performance liquid chromatography (HPLC) is of particular importance. Of particular importance
is Hb E, which is the most common and the most significant variant. The aim of this study was to
study a rare variant infrequently seen in our countries during the routine work.
MATERIALS AND METHODS: Sixteen Bengali workers at Najran University Hospital, Saudi Arabia,
came to the laboratory for routine investigation. CBC, routine blood chemistry, and Hb separation
by HPLC were performed.
RESULTS: Three cases out of 16 showed an abnormal Hb peaked on the A2 window on HPLC
consistent with the diagnosis of Hb E. Two of them had Hb E of 29.1% of each. The third case had
Hb E around 86%. In addition, one case was consistent with β thalassemia trait had increased Hb
A2 of 5.7%. Five cases were borderline.
CONCLUSION: HbE could be adequately differentiated from other Hb variants eluting in the A2
window on HPLC by the percentage of the variant, its retention time, the mild clinical presentation,
and the ethnic origin of the patient.