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dc.contributor.authorLUKANMBI, F. A-
dc.contributor.authorADEYOKUNNU, I. A. A.-
dc.contributor.authorBOLA, O-
dc.contributor.authorOSIFO, A-
dc.contributor.authorBOLODEOKU, J. O.-
dc.contributor.authorDADA, O. A.-
dc.date.accessioned2024-08-14T10:30:40Z-
dc.date.available2024-08-14T10:30:40Z-
dc.date.issued1986-
dc.identifier.citationAfr. J. Med. med. Sci. (1986) 15, 25-28en_US
dc.identifier.issn1116-4077-
dc.identifier.urihttp://adhlui.com.ui.edu.ng/jspui/handle/123456789/2659-
dc.descriptionARTICLEen_US
dc.description.abstractThyroid function was assessed in ninety children with homozygous sickle-cell disease (haemoglobin genotype SS) in forty-five children with heterozygous sickle-cell trait (AS) and in 162 control children with haemoglobin genotype A A. Serum levels of thyroxine, the invitro triidothyroninc resin uptake and the calculated index of free thyroxine* were not significantly different in the three groups. The distribution of individual thyrotropin (TSII) values showed that only 11% of the HbSS subjects had values below the 95% confidence limits for the HbA A controls. However, the mean level of TSII was significantly lower in the HbSS than the other two groups of childrenen_US
dc.description.sponsorshipCOLLEGE OF MEDICINEen_US
dc.language.isoenen_US
dc.publisherBLACKWELL SCIENTIFIC PUBLICATIONSen_US
dc.subjectHaemoglobinopathiesen_US
dc.subjectBiochemical assessmenten_US
dc.subjectThyroid functionen_US
dc.subjectSickle-cell diseaseen_US
dc.titleEndocrine function and haemoglobinopathies: biochemical assessment of thyroid function in children with sickle-cell diseaseen_US
dc.typeArticleen_US
Appears in Collections:African Journal of Medicine and Medical Sciences

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