alexa Abstract | High Hemoglobin F in a Saudi Child Presenting with Pancytopenia

Journal of Pediatric Care
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Case Report Open Access


Saudi Arabia has a high prevalence of sickle cell disease with a wide spectrum of clinical presentations, and sickle cell disease patients are divided according to the clinical phenotypes. Sickle cell disease patients who have higher expression of hemoglobin F level are reported to experience milder disease since high hemoglobin F is thought to ameliorate the disease manifestations. However, the effects are not consistent since hemoglobin F is not equally distributed among erythrocytes. Multiple factors can help determine the level of fetal hemoglobin in adults. Here we report a case of a Saudi patient who presented with her first crisis at the age of 6 years.

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Author(s): Abdullah A Elhosiny Alaa E Kintab Soheir S Adam


Sickle Cell Disease, High Hemoglobin F, Neonatal Care, Pediatric Neurology, Pediatric Dermatology, Pediatric Dental Care, Pediatric Oncology, Pediatric Urology, Pediatric Cardiology, Pediatric Hematology, Pediatric Nephrology, Pediatric Orthopedics, Pediatric Endocrinology, Prenatal ethical considerations, Pediatric Gastroenterology, Gynecology

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