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1983 1
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Page 1
Congenital adrenal hyperplasia in pregnancy.
Garner PR. Garner PR. Semin Perinatol. 1998 Dec;22(6):446-56. doi: 10.1016/s0146-0005(98)80025-6. Semin Perinatol. 1998. PMID: 9880115 Review.
During pregnancy, maternal and fetal problems are confined to women who have 21-hydroxylase deficiency (P450c21 deficiency), 11-hydroxylase deficiency (P450c11 deficiency), and 3 beta-hydroxysteroid dehydrogenase deficiency (3 beta HSD deficienc …
During pregnancy, maternal and fetal problems are confined to women who have 21-hydroxylase deficiency (P450c21 deficiency), 11-hydroxylase …
The incidence of late-onset congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency among hirsute women.
Mathieson J, Couzinet B, Wekstein-Noel S, Nahoul K, Turpin G, Schaison G. Mathieson J, et al. Clin Endocrinol (Oxf). 1992 Apr;36(4):383-8. doi: 10.1111/j.1365-2265.1992.tb01464.x. Clin Endocrinol (Oxf). 1992. PMID: 1330378
OBJECTIVE: The present study was designed to determine the incidence of 3 beta-hydroxysteroid dehydrogenase deficiency (3 beta-HSD) in adult women with hyperandrogenism. ...
OBJECTIVE: The present study was designed to determine the incidence of 3 beta-hydroxysteroid dehydrogenase d …
Ambiguous genitalia: two decades of experience.
Al-Jurayyan NA. Al-Jurayyan NA. Ann Saudi Med. 2011 May-Jun;31(3):284-8. doi: 10.4103/0256-4947.81544. Ann Saudi Med. 2011. PMID: 21623059 Free PMC article.
Male genetic sex (46XY) was present in only 28 (34.6%) patients with a diversity of causes; multiple congenital anomalies in 9 (32.1%), local anorectal anomalies in 2 (7.1%), congenital adrenal hyperplasia (3-beta-hydroxysteroid dehydrogenase defici …
Male genetic sex (46XY) was present in only 28 (34.6%) patients with a diversity of causes; multiple congenital anomalies in 9 (32.1%), loca …
Absence of nonclassical congenital adrenal hyperplasia in patients with precocious adrenarche.
Morris AH, Reiter EO, Geffner ME, Lippe BM, Itami RM, Mayes DM. Morris AH, et al. J Clin Endocrinol Metab. 1989 Oct;69(4):709-15. doi: 10.1210/jcem-69-4-709. J Clin Endocrinol Metab. 1989. PMID: 2550505
Stimulated 11-deoxycortisol values [less than 400 ng/dL (11.6 nmol/L)] ruled out any cases of nonclassical 11 beta-hydroxylase deficiency. No patient had nonclassical 3 beta-hydroxysteroid dehydrogenase deficiency, as defined by both the stimula …
Stimulated 11-deoxycortisol values [less than 400 ng/dL (11.6 nmol/L)] ruled out any cases of nonclassical 11 beta-hydroxylase deficiency. N …
Isolated precocious pubarche: an approach.
Balducci R, Boscherini B, Mangiantini A, Morellini M, Toscano V. Balducci R, et al. J Clin Endocrinol Metab. 1994 Aug;79(2):582-9. doi: 10.1210/jcem.79.2.8045980. J Clin Endocrinol Metab. 1994. PMID: 8045980
Seven of 112 patients (6.2%) were diagnosed as having nonclassical 3 beta-hydroxysteroid dehydrogenase deficiency (NC3HSD) on the basis of the following three criteria: stimulated 17PGN levels and stimulated 17PGN/17OHP and 17PGN/cortisol ratios …
Seven of 112 patients (6.2%) were diagnosed as having nonclassical 3 beta-hydroxysteroid dehydrogenase defici …
Testis sparing surgery for steroid unresponsive testicular tumors of the adrenogenital syndrome.
Walker BR, Skoog SJ, Winslow BH, Canning DA, Tank ES. Walker BR, et al. J Urol. 1997 Apr;157(4):1460-3. J Urol. 1997. PMID: 9120982 Clinical Trial.
MATERIALS AND METHODS: Four boys with steroid unresponsive testicular tumors of the adrenogenital syndrome were evaluated with MRI, testicular ultrasound and color flow Doppler examinations preoperatively and postoperatively. Three patients had 21-hydroxylase deficiency and 1 had …
MATERIALS AND METHODS: Four boys with steroid unresponsive testicular tumors of the adrenogenital syndrome were evaluated with MRI, testicul …
15 results