Title of article
The Clinical Approach toward Hereditary Persistence of Fetal Hemoglobin: A Case Report
Author/Authors
Ghaderi ، Afshin Department of Internal Medicine, Hematology and Medical Oncology Ward - Yasuj University of Medical Sciences , Bakhtiari ، Tahereh Department of Immunology - School of Medicine - Isfahan University of Medical Sciences , Jokar ، Saeid Department of Internal Medicine - Shahids Rajaee Hospital of Gachsaran - Yasuj University of Medical Sciences , Eshraghi ، Abbas Department of Internal Medicine - Qom University of Medical Sciences
From page
364
To page
368
Abstract
Fetal hemoglobin is the principal hemoglobin in the human fetus, and the adult levels of fetal hemoglobin (HbF) are less than 1% of total hemoglobin. A steady increase of HbF in patients with hereditary persistence of fetal hemoglobin (HPFH) is associated with complications. The present report describes HPFH in a 26-year-old man with emphasis on its hemoglobin electrophoresis. The patient was admitted with complaints of recurrent weakness and lethargy, weight loss, abdominal pain, and dyspepsia. Splenectomy was planned due to massive splenomegaly and gastrointestinal complications. Ultimately, electrophoresis confirmed the diagnosis of HPFH.
Keywords
Blood protein electrophoresis , Fetal hemoglobin , Hemoglobinopathies
Journal title
Iranian Journal of Allergy, Asthma and Immunology
Journal title
Iranian Journal of Allergy, Asthma and Immunology
Record number
2721823
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