| Literature DB >> 8463907 |
Abstract
Three children with homozygous sickle cell disease, 22 months and 8 and 10 years of age, had clinical and hematologic manifestations of aplastic and splenic sequestration crisis simultaneously. They had an acute drop in hemoglobin level (16, 20, and 45 gm/L), reticulocytopenia (0.1%, 0.6%, and 0.3%), and sudden splenic enlargement. Evidence of recent parvovirus infection was demonstrated.Entities:
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Year: 1993 PMID: 8463907 DOI: 10.1016/s0022-3476(05)83542-5
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406