id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_3m3emadx65e6toqpgjdfrh6gqu	M. I. New	Steroid disorders in children: Congenital adrenal hyperplasia and apparent mineralocorticoid excess	1999	8	.pdf	application/pdf	8783	1348	74	precursors accumulate in excess and are converted to potent androgens, which are secreted and cause in utero virilization of the affected female fetus genitalia in the classical form of CAH. potentially fatal genetic disorder causing severe juvenile hypertension, preand postnatal growth failure, and low to undetectable recessive mutations in the HSD11B2 gene, which result in a deficiency excess; ACTH, adrenocorticotropic hormone; 11b-HSD2, 11b-hydroxysteroid dehydrogenase type 2; 21-OHD, 21-hydroxylase deficiency; 17-OHP, 17a-hydroxyprogesterone; MR, AME is a genetic disorder that typically causes severe hypertension in children, preand HSD11B2 gene in patients affected with AME (Fig. 7) (refs. have recently reported the first patient with a mild form of AME. Review of AME patients studied at the New York Hospital–Cornell Medical Center: Signs and biochemical features at S., Dupont, B., Lorenzen, F., Pang, S., Pollack, M., Oberfield, S. S., Dupont, B., Lorenzen, F., Pang, S., Pollack, M., Oberfield, S.	./cache/work_3m3emadx65e6toqpgjdfrh6gqu.pdf	./txt/work_3m3emadx65e6toqpgjdfrh6gqu.txt