Analysis of glucocorticoid metabolites in the neonatal period: Catabolism of cortisone acetate by an infant with 21-hydroxylase deficiency

The urinary excretion of 27 individual 17-hydroxycorticosteroids by a female infant with 21-hydroxylase deficiency was studied using gas chromatography on an open-tubular column and combined gas chromatography-mass spectrometry. Samples were analysed from days 1, 3 and 4 of life, before cortisone ac...

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Veröffentlicht in:	Clinica chimica acta 1978-05, Vol.85 (3), p.219-229
Hauptverfasser:	Taylor, N.F., Curnow, D.H., Shackleton, C.H.L.
Format:	Artikel
Sprache:	eng
Schlagworte:	17-Hydroxycorticosteroids - urine Adrenal Hyperplasia, Congenital Chromatography, Gas Cortisone - analogs & derivatives Cortisone - metabolism Cortisone - therapeutic use Female Humans Infant, Newborn Mass Spectrometry Steroid Hydroxylases - deficiency
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