A rare cause of coma in pediatric patients: Beta-ketothiolase (2-methylacetoacetyl-Co A thiolase) deficiency [Çocuklarda komanin nadir bir nedeni: Beta-ketotiyolaz (2-metilasetoasetil-koenzim A tiyolaz) eksikli?i]

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dc.contributor.authorÜnal E.
dc.contributor.authorGüzeş E.A.
dc.contributor.authorAydin K.
dc.contributor.authorKaya Ü.
dc.contributor.authorEnergin M.
dc.date.accessioned2020-03-26T17:18:49Z
dc.date.available2020-03-26T17:18:49Z
dc.date.issued2007
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractBeta-ketothiolase deficiency is a rare inborn error of L-isoleucine catabolism and ketone body metabolism. We present a 13-month-old, girl with beta-ketothiolase deficiency who was admitted with rapidly progressive coma. Severe ketoacidosis and mild hyperammonemia was documented. This rare case was treated successfully during the acute episode.en_US
dc.identifier.endpage79en_US
dc.identifier.issn1306-0015en_US
dc.identifier.issue2en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage77en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/21745
dc.identifier.volume42en_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.publisherKare Publishingen_US
dc.relation.ispartofTurk Pediatri Arsivien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectBeta-ketothiolase deficiencyen_US
dc.subjectComaen_US
dc.subjectKetoacidosisen_US
dc.titleA rare cause of coma in pediatric patients: Beta-ketothiolase (2-methylacetoacetyl-Co A thiolase) deficiency [Çocuklarda komanin nadir bir nedeni: Beta-ketotiyolaz (2-metilasetoasetil-koenzim A tiyolaz) eksikli?i]en_US
dc.typeArticleen_US

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