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J Inherit Metab Dis ; 30(5): 735-42, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17603756

ABSTRACT

Transaldolase deficiency, a recently discovered disorder of carbohydrate metabolism with multisystem involvement, has been diagnosed in 6 patients. Affected patients have abnormal concentrations of polyols in body fluids and in all patients we have previously found increased amounts of a seven-carbon chain carbohydrate which we suspected of being sedoheptulose. We report development of a liquid chromatography-tandem mass spectrometry method for quantitation of the seven-carbon carbohydrates sedoheptulose and mannoheptulose in urine. Additionally, other seven-carbon chain carbohydrates were characterized in urine, including sedoheptitol, perseitol and sedoheptulose 7-phosphate. Transaldolase-deficient patients had significantly increased urinary sedoheptulose and sedoheptulose 7-phosphate, associated with subtle elevations of mannoheptulose, sedoheptitol and perseitol. Our findings reveal novel urinary biomarkers for identification of transaldolase deficiency.


Subject(s)
Carbohydrate Metabolism, Inborn Errors/diagnosis , Chromatography, Liquid , Heptoses/urine , Tandem Mass Spectrometry , Transaldolase/deficiency , Urinalysis/methods , Adolescent , Adult , Aged , Biomarkers/urine , Carbohydrate Metabolism, Inborn Errors/enzymology , Carbohydrate Metabolism, Inborn Errors/genetics , Carbohydrate Metabolism, Inborn Errors/urine , Child , Child, Preschool , Chromatography, Liquid/standards , Female , Humans , Infant , Infant, Newborn , Male , Mannoheptulose/urine , Middle Aged , Reference Values , Reproducibility of Results , Sugar Phosphates/urine , Tandem Mass Spectrometry/standards , Transaldolase/genetics , Urinalysis/standards
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