Renal hemosiderosis complicating sickle cell anemia
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چکیده
منابع مشابه
Renal hemosiderosis complicating sickle cell anemia.
A 37-year-old Brazilian black male with a history of sickle cell anemia presented with a 2-week history of pain and edema in the lower extremities, accompanied by generalized weakness and dyspnea on exertion. Outpatient laboratory evaluation revealed hemoglobin of 4.3 mg/dl, creatinine of 5.8 mg/dl, and blood urea nitrogen of 100 mg/dl. Ten months prior to admission, he had been hospitalized fo...
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INTRODUCTION Pyomyositis is a bacterial infection of skeletal muscle and a rare complication of sickle cell anemia. It may present a difficult problem in diagnosis, leading to delay in appropriate treatment and development of complications including abscess formation and osteomyelitis. CASE PRESENTATION We report the case of a 44-year-old Afro-Caribbean woman with homozygous sickle cell disea...
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Background: Hemoglobin S arises is the result of a point mutation (A-T) in the sixth codon on the -globin gene on chromosome 11 causing sickle cell anemia. The presence of fetal hemoglobin in infancy plays a relatively protective role for vaso-occlusive symptoms that are the major contributor for the morbidity and mortality among patients with sickle cell anemia. hydroxyurea, an s-phase-specif...
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Patients with sickle cell anemia (Hb SS) or sickle cell trait (Hb AS) may present several types of renal dysfunction; however, comparison of the prevalence of these abnormalities between these two groups and correlation with the duration of disease in a large number of patients have not been thoroughly investigated. In a cross-sectional study using immunoenzymometric assays to measure tubular p...
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ژورنال
عنوان ژورنال: Kidney International
سال: 2012
ISSN: 0085-2538
DOI: 10.1038/ki.2011.470