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dc.contributor.authorLUKANMBI, F. A.-
dc.contributor.authorADEYOKUNNU, A. A.-
dc.contributor.authorOSIFO, B. O. A.-
dc.contributor.authorBOLODEOKU, J. O.-
dc.contributor.authorDADA, O. A.-
dc.date.accessioned2023-02-03T11:03:19Z-
dc.date.available2023-02-03T11:03:19Z-
dc.date.issued1986-03-
dc.identifier.citationAfr. J. Med. med. Sci. (1986) 15(1/2): 25-28.en_US
dc.identifier.issn1116-4077-
dc.identifier.urihttp://adhlui.com.ui.edu.ng/jspui/handle/123456789/1874-
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 AA. Serum levels of thyroxine, the in vitro triidothyronine resin uptake, and the calculated index of "free thyroxine" were not significantly different in the three groups. The distribution of individual thyrotropin (TSH) values showed that only 11% of the HbSS subjects had values below the 95% confidence limits for the HbAA controls. However, the mean level of TSH 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.publisherCOLLEGE OF MEDICINEen_US
dc.subjectThyroiden_US
dc.subjectGenotypeen_US
dc.subjectChildrenen_US
dc.subjectSickle-cell diseaseen_US
dc.subjectHaemoglobinen_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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