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the clinical approach toward hereditary persistence of fetal hemoglobin: a case report
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نویسنده
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ghaderi afshin ,bakhtiari tahereh ,jokar saeid ,eshraghi abbas
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منبع
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iranian journal of allergy, asthma and immunology - 2022 - دوره : 21 - شماره : 3 - صفحه:364 -368
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چکیده
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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.
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کلیدواژه
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blood protein electrophoresis ,fetal hemoglobin ,hemoglobinopathies
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آدرس
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yasuj university of medical sciences, department of internal medicine, hematology and medical oncology ward, iran, isfahan university of medical sciences, school of medicine, department of immunology, iran, yasuj university of medical sciences, shahids rajaee hospital of gachsaran, department of internal medicine, iran, qom university of medical sciences, department of internal medicine, iran
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پست الکترونیکی
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ae845@yahoo.com
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Authors
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