๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Diagnosis of 21-hydroxylase deficiency in newborn infants by GC-MS of urinary steroids

โœ Scribed by A. B. W. YONG; J. J. PITT; J. MONTALTO; H. E. DAVIES; G. L. WARNE; J. F. CONNELLY


Book ID
118706179
Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
510 KB
Volume
24
Category
Article
ISSN
1034-4810

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Two-Step Biochemical Differential Diagno
โœ Koyama, Y.; Homma, K.; Fukami, M.; Miwa, M.; Ikeda, K.; Ogata, T.; Hasegawa, T.; ๐Ÿ“‚ Article ๐Ÿ“… 2012 ๐Ÿ› American Association for Clinical Chemistry ๐ŸŒ English โš– 374 KB
Detection of late onset steroid 21-hydro
โœ J. Homoki; J. Solyom; W. M. Teller ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Springer ๐ŸŒ English โš– 513 KB

Patients suffering from late onset 21-hydroxylase deficiency (LO-CAH) excreted only slightly higher amounts of 17-hydroxypregnanolone (17-OH-PO), pregnanetriol (PT) and 11-oxo-pregnanetriol (11-O-PT) than age-matched healthy controls. To discriminate between LO-CAH and virilization of unknown origin