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17- alpha hydroxylase deficiency

G-13) (G-13) 17-alpha hydroxylase deficiency. I here is a decrease in both glucocorticoid and androgen production. The mineralocorticoid path is open and this may cause hypertension through excess mineralocorticoids. [Pg.53]

Jansen, G.A., Mihalik, SJ., Watkins, P.A., Moser, H.W., Jakobs, C, Denis, S. Wanders, R.J.A. (19%) Biochem. Biophys. Res. Commun. 229, 205-210. Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humans. [Pg.295]


See other pages where 17- alpha hydroxylase deficiency is mentioned: [Pg.345]    [Pg.1068]   
See also in sourсe #XX -- [ Pg.45 ]




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