Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4658
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dc.contributor.authorCanatan, D.-
dc.contributor.authorBagcı, Hüseyin.-
dc.contributor.authorGumuslu, S.-
dc.contributor.authorBilmen, S.-
dc.contributor.authorAçıkbaş, İbrahim.-
dc.contributor.authorBalta, N.-
dc.contributor.authorOguz, N.-
dc.date.accessioned2019-08-16T11:36:00Z
dc.date.available2019-08-16T11:36:00Z
dc.date.issued2006-
dc.identifier.issn1108-2682-
dc.identifier.urihttps://hdl.handle.net/11499/4658-
dc.description.abstractGlucose-6-phosphate dehydrogenase deficiency (G6PD) in south of Turkey is a very important health problem; the incidence of G6PD was reported 5, 4-20% by the surveillance studies. Patients with favism are admitted to urgent hospital service after ingestion of vicia faba beans especially at the spring season. Aim of this study was to investigate patients with favism who had a history of consumed fava as clinical, haematological, biochemical and mutations. Fifty patients, aged 1-16 years (mean±SD: 5.94±4.54 years), 40 males (80%) and 10 females (20%) were included in this study. The complaints of them were pale (100%), icterus (84%), haemoglobinuria (72%), abdominal pain (60%) and fever (4%). In their history they had neonatal hyperbilurubinaemia (40%) repeated acute haemolysis (10%) and chronic non-spherocytic haemolytic anaemia (6%). G6PD activities were ranging from a complete deficiency in 10 (20%), moderate in 12 (24%), mild in 5 (10%) to normal levels in 23 patients (46%). Molecular studies of the patients were detected in 35 subjects (70%); only Mediterranean mutations were detected (563T). In conclusion, our patients with favism had the same complaints and clinical findings with other G6PD patients but their biochemical enzyme levels were heterogeneous and the incidence of Mediterranean mutation was high. Copyright © Hellenic Society of Haematology.en_US
dc.language.isoenen_US
dc.relation.ispartofHAEMAen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectFavismen_US
dc.subjectG6PDen_US
dc.subjectMediterranean mutationsen_US
dc.subjectTurkeyen_US
dc.subjectglucose 6 phosphate dehydrogenaseen_US
dc.subjectabdominal painen_US
dc.subjectadolescenten_US
dc.subjectanamnesisen_US
dc.subjectarticleen_US
dc.subjectblood examinationen_US
dc.subjectchemical analysisen_US
dc.subjectchilden_US
dc.subjectclinical articleen_US
dc.subjectclinical featureen_US
dc.subjectclinical studyen_US
dc.subjectcontrolled studyen_US
dc.subjectfavismen_US
dc.subjectfemaleen_US
dc.subjectfeveren_US
dc.subjectgene mutationen_US
dc.subjectglucose 6 phosphate dehydrogenase deficiencyen_US
dc.subjecthemoglobinuriaen_US
dc.subjecthemolysisen_US
dc.subjecthemolytic anemiaen_US
dc.subjecthumanen_US
dc.subjecthyperbilirubinemiaen_US
dc.subjectjaundiceen_US
dc.subjectmaleen_US
dc.subjectpalloren_US
dc.subjectTurkey (republic)en_US
dc.titleThe features of patients with favism in Turkeyen_US
dc.typeArticleen_US
dc.identifier.volume9en_US
dc.identifier.issue2en_US
dc.identifier.startpage247
dc.identifier.startpage247en_US
dc.identifier.endpage250en_US
dc.authorid0000-0001-7483-1147-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-33744962608en_US
dc.identifier.scopusqualityQ4-
dc.ownerPamukkale_University-
item.openairetypeArticle-
item.grantfulltextnone-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.03. Basic Medical Sciences-
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
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