GP CHROUSOS, D Loriaux, DL MANN, GB … - Annals of Internal …, 1982 - Am Coll Physicians The importance of late-onset congenital adrenal hyperplasia as a cause of hirsutism is
controversial. Two of 35 women with a chief complaint of hirsutism met the criteria of 21-hydroxylase
deficiency. In one, who presented with hirsutism, oligomenorrhea, obesity, infertility, and ... Cited by 76 - Related articles - All 2 versions
RA Lobo, U Goebelsmann - American journal of obstetrics and …, 1980 - ncbi.nlm.nih.gov This study was carried out to document the postpubertal presentation of congenital adrenal hyperplasia
(CAH), to elaborate the diagnostic criteria for it, and to investigate family members of CAH
patients. Serum 17-hydroxyprogesterone (17OHP) was measured in normal women and ... Cited by 65 - Related articles
F Kuttenn, P Couillin, F Girard, L Billaud, M … - New England Journal …, 1985 - content.nejm.org We studied the incidence of late-onset adrenal hyperplasia as a cause of hirsutism, its association
with the major histocompatibility complex, and its clinical expression. Twenty-four of 400 women
seen because of hirsutism were found to have late-onset adrenal hyperplasia, diagnosed ... Cited by 104 - Related articles - All 3 versions
RJ CHETKOWSKI, J DEFAZIO, I SHAMONKI, … - Journal of Clinical …, 1984 - Endocrine Soc Late-onset congenital adrenal hyperplasia (CAH) due to 21-hydroxyklase deficiency is a cause
of hirsutism in adult women. Its reported frequency of occurrence in hirsute women has varied
from 0–30%, but the number of patients studied was small. To establish the incidence of ... Cited by 58 - Related articles - All 3 versions
B KOHN, LS LEVINE, MS POLLACK, S PANG, … - Obstetrical & …, 1983 - journals.lww.com 494 Obstetrical and Gynecological Survey been reported previously. These families are referred
to as A, B, C, D, E, F, H, and I. HLA genotyping revealed four siblings (E 11-2, F 11-2, G 11-2,
and I 11-2) who were HLA- identical (haplotypes a/c) to the affected patients within their ... Cited by 105 - Related articles - All 2 versions
CJ MIGEONE, ZEV ROSENWAKS, PA LEE, … - Obstetrical & …, 1981 - journals.lww.com Genetics 143 amounts of estradiol or esterone, as well as testosterone, but clinical experience
seems to indicate that androstendione is the major ste- roid from the menopausal ovary and
that this is converted in the periphery to estrone, the significant menopausal ... Cited by 42 - Related articles - All 2 versions
JL Gabrilove, DC Sharma, RI Dorfman - The New England journal of …, 1965 - ncbi.nlm.nih.gov 1: N Engl J Med. 1965 Jun 10;272:1189-94. ADRENOCORTICAL 11-BETA-
HYDROXYLASE DEFICIENCY AND VIRILISM FIRST MANIFEST IN THE ADULT
WOMEN. GABRILOVE JL, SHARMA DC, DORFMAN RI. Mesh Terms ... Cited by 42 - Related articles
DF Child, DE Bu'Lock, DC Anderson - Clin. Endocrinol, 1980 - interscience.wiley.com Adrenal steroidogenesis has been studied in vivo in ten hirsute and ten normal women. Serum
levels of nine steroids on the biosynthetic pathway: the Δ 5 3 β-hydroxysteroids, pregnenolone
(Pe), 17α-hydroxypregnenolone (17 Pe), dehydroepiandrosterone (DHEA), ... Cited by 23 - Related articles - All 2 versions
… -HAUDIQUET, C SAINSARD, J BUVAT, JP … - Journal of Clinical …, 1986 - Endocrine Soc We analyzed data from 20 patients with lateonset 21-hydroxylase deficiency (LOHD). Three clinical
phenotypes could be distinguished among the 18 women. Seven (39%) presented with clinical
features suggesting polycystic ovarian disease (PCOD). However, despite androgen ... Cited by 81 - Related articles - All 3 versions
GP Chrousos, DL Loriaux, D Mann, GB Cutler Jr - Horm Res, 1982 - content.karger.com Three families with late-onset 21 -hydroxylase deficiency were studied. Homozygous females
presented with symptoms of mild hyperandrogenism such as acne, hirsutism, oligomenorrhea
and menometrorrhagia. A homozygous male was asymptomatic and had reached normal ... Cited by 20 - Related articles - All 4 versions
