Incidence of overt and covert neurological damage in children with sickle cell disease
Open Access
- 1 September 1987
- journal article
- research article
- Published by Oxford University Press (OUP) in Postgraduate Medical Journal
- Vol. 63 (743) , 751-753
- https://doi.org/10.1136/pgmj.63.743.751
Abstract
Summary: We studied 25 patients with sickle cell disease (15 with HbSS; 8 with HbSC and 2 with HbS beta degree) using neurological examination as a marker of overt and computed tomographic (CT) scan as a marker of covert neurological damage. Of the 25 patients, 5 (20%) had evidence of cerebral infarcts on CT scan, but only 4 of these 5 patients had neurological signs. Neurological problems were only seen in patients with HbSS. We could not identify any haematological risk factors, but in this small group of HbSS patients a crisis rate greater than 1 per year of follow up was associated with a significant risk of neurological damage.This publication has 14 references indexed in Scilit:
- Hematologically and Genetically Distinct Forms of Sickle Cell Anemia in AfricaNew England Journal of Medicine, 1985
- Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia?1984
- Neurological Complications of Hemoglobin SC DiseaseArchives of Neurology, 1984
- STROKE IN CHILDREN. CLINICAL CHARACTERISTICS AND PROGNOSISActa Paediatrica, 1983
- The Interaction of Alpha-Thalassemia and Homozygous Sickle-Cell DiseaseNew England Journal of Medicine, 1982
- Concurrent Sickle-Cell Anemia and α-ThalassemiaNew England Journal of Medicine, 1982
- Neurological complications of sickle cell anemiaJournal of Pediatric Hematology/Oncology, 1982
- Efficacy of transfusion therapy for one to two years in patients with sickle cell disease and cerebrovascular accidentsThe Journal of Pediatrics, 1980
- Periodic Transfusions for Sickle Cell Anemia and CNS InfarctionArchives of Pediatrics & Adolescent Medicine, 1979
- The natural history of stroke in sickle cell diseaseThe American Journal of Medicine, 1978