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Adrenogenital syndrome deficiency

Bongiovanni AM (1962) The adrenogenital syndrome with deficiency of 3/ -hydroxysteroid dehydrogenase. J Clin Invest 41 2086-2092... [Pg.600]

Steroid 21-hydroxylase deficiency is the most commonly encountered form of the adrenogenital syndrome and has been widely studied using a... [Pg.51]

Figure 51-15 Formation of steroids in patients with adrenogenital syndrome caused by 21 -hydroxylase deficiency. Bold lettering indicates steroids that are found elevated in the circulation. ACTH, Adrenocorticotropic hormone SpSDH 3p-hydroxysteroid dehydrogenase. Figure 51-15 Formation of steroids in patients with adrenogenital syndrome caused by 21 -hydroxylase deficiency. Bold lettering indicates steroids that are found elevated in the circulation. ACTH, Adrenocorticotropic hormone SpSDH 3p-hydroxysteroid dehydrogenase.
Wudy SA, Homoki J, Wachter UA, Teller WM. Diagnosis of the adrenogenital syndrome caused by llp-hydroxylase deficiency using gas chromatographic-mass spectrometric analysis of the urinary steroid profile. Dtsch Med Wochenschr 1997 122 3-11. [Pg.2051]

See other pages where Adrenogenital syndrome deficiency is mentioned: [Pg.549]    [Pg.904]    [Pg.2028]    [Pg.83]    [Pg.160]    [Pg.643]   
See also in sourсe #XX -- [ Pg.77 ]



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