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dc.contributor.authorAkenami, F.O.T-
dc.contributor.authorAken'Ova, Y.A-
dc.contributor.authorOsifo, B.O-
dc.date.accessioned2025-03-05T12:42:12Z-
dc.date.available2025-03-05T12:42:12Z-
dc.date.issued1999-
dc.identifier.citationAfr. J. Med. Med. Sci. (1999) 28, 137-139en_US
dc.identifier.issn1116-4077-
dc.identifier.urihttp://adhlui.com.ui.edu.ng/jspui/handle/123456789/3500-
dc.descriptionArticleen_US
dc.description.abstractSerum zinc, copper and magnesium were studied in patients with sickle cell disease in the steady state. There was significantly lower scrum zinc concentration (P < 0.01) and significantly higher serum copper and magnesium in hemoglobin S patients compared with controls (HbA). In hemoglobin SC patients, there was a significant reduction in serum zinc (P< 0.01) but no significant difference in serum copper and magnesium concentrations compared with the controls. There was no significant difference in serum zinc concentration between the HbS and HbS+C patients. However, there were significantly higher scrum copper and magnesium in HbS than HbS+C patients (P < 0.01) The level of serum zinc has no correlation with the steady state Hematocrit or severity index score in HbS and HbS+C patientsen_US
dc.description.sponsorshipCOLLEGE OF MEDICINE, UNIVERSITY OF IBADAN, NIGERIAen_US
dc.language.isoenen_US
dc.publisherCOLLEGE OF MEDICINE, UNIVERSITY OF IBADAN, NIGERIAen_US
dc.subjectZincen_US
dc.subjectCopperen_US
dc.subjectSteady stateen_US
dc.subjectMagnesiu-sickle cell diseaseen_US
dc.titleSerum zinc, copper and magnesium in sickle cell disease at Ibadan, South Western Nigeriaen_US
dc.typeArticleen_US
Appears in Collections:African Journal of Medicine and Medical Sciences

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