Glomerular function and hyperuricaemia in sickle cell disease.

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Glomerular function and hyperuricaemia in sickle cell disease.

Renal insufficiency is common in adults with homozygous sickle cell disease, and the contribution of glomerular failure to the hyperuricaemia which is often a feature of the disease has therefore been investigated. In a study of 64 patients between the ages of 15 and 66, serum urate concentration was dependent on renal urate clearance and also on creatinine clearance. The relation between serum...

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Glomerular hyperfiltration in sickle cell disease.

S ickle cell disease (SCD) is a monogenetic, chronic anemia syndrome that is caused by a point mutation in the -globin gene and affects approximately 100,000 individuals in the United States. Approximately 4 to 5% of these individuals have or will develop stage 5 chronic kidney disease (CKD), and 0.11% of patients who are on long-term maintenance renal replacement therapy have SCD-associated ne...

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In patients with sickle cell disease, thrombotic microangiopathy is a rare complication. Also in sickle cell disease, intracardiac thrombus formation without structural heart diseases or atrial arrhythmias is a rare phenomenon. We herein describe a 22-year-old woman, who was a known case of sickle cell-βthalassemia, had a history of recent missed abortion, and was admitted with a vaso-occlusive...

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Neonatal Screening for Sickle Cell Disease in Southwest Iran

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ژورنال

عنوان ژورنال: Journal of Clinical Pathology

سال: 1984

ISSN: 0021-9746

DOI: 10.1136/jcp.37.9.1046