Hypothalamic-pituitary-thyroidal axis dysfunction and cortisol secretion in patients with nonclassical congenital adrenal hyperplasia

International Journal of Fertility and Women's Medicine

Volumn 46, Issue 1, 2001, Pages 37-41

  Trakakis, E ^a   Chryssikopoulos, A ^a   Sarandakou, A ^a   Phocas, I ^a   Rizos, D ^a   Gregoriou, O ^a   Kontoravdis, A ^a   Creatsas, G ^a  

^a UNIVERSITY OF ATHENS   (Greece)

Author keywords

21 hydroxylase deficiency; ACTH secretion; Infertility (female)

Indexed keywords

CORTICOTROPIN; HLA ANTIGEN; HYDROCORTISONE; HYDROXYPROGESTERONE; LIOTHYRONINE; THYROID HORMONE; THYROTROPIN; THYROXINE;

ACNE; ADULT; ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; FEMALE; FEMALE INFERTILITY; FREE THYROXINE INDEX; HAPLOTYPE; HIRSUTISM; HORMONE DETERMINATION; HUMAN; HYDROCORTISONE RELEASE; HYPERANDROGENISM; HYPOTHALAMUS HYPOPHYSIS THYROID SYSTEM; MAJOR CLINICAL STUDY; MENSTRUAL CYCLE; MENSTRUAL IRREGULARITY; PRIORITY JOURNAL; SEBORRHEA; STEROID 21 MONOOXYGENASE DEFICIENCY; THYROID FUNCTION;

17-ALPHA-HYDROXYPROGESTERONE; ADRENAL HYPERPLASIA, CONGENITAL; ADRENOCORTICOTROPIC HORMONE; ADULT; FEMALE; HUMANS; HYDROCORTISONE; HYPERANDROGENISM; HYPOTHALAMO-HYPOPHYSEAL SYSTEM; THYROID FUNCTION TESTS; THYROID GLAND; THYROID HORMONES; THYROTROPIN;

EID: 0034916239     PISSN: 1534892X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (29)

1. The adrenal hyperplasias
2. CAH caused by 21-hydroxylase deficiency
3. Genotyping steroid 21-hydroxylase deficiency: Hormonal reference data
4. Clinical review 54. Genetics, diagnosis and management of 21-hydroxylase deficiency
5. Clinical review 56. Nonclassical adrenal hyperplasia: Current concepts
6. Spontaneous thyrotropin and cortisol secretion interactions in patients with nonclassical 21-hydroxylase deficiency and control children
7. The functions of corticosteroid-binding-globulin and sex hormone-binding-globulin: Recent advances
8. Thyroid disease and reproductive dysfunction: A review
9. Changes in thyroid function tests during danazol therapy
10. The concepts of stress and stress system disorders
11. Evaluation of hypothalamo-pituitary adrenocortical function in children by human corticotropin-releasing hormone (MCI-028) test
12. Glucocorticoids and thyrotropin releasing hormone (TRH) secretion
13. The role of glucocorticoid in the regulation of thyrotropin
14. Inhibition of thyrotropin secretion by physiological levels of corticosterone
15. Pituitary-adrenal responses to corticotropin-releasing hormone in different degrees of adrenal 21-hydroxylase deficiency
16. Familial study of hirsutism
17. The incidence of la-hydroxylase deficiency in Greek hyperandrogenic women. Screening and diagnosis
18. A contribution to the classification of cases of nonclassic 21-hydroxylase deficient congenital adrenal hyperplasia
19. New reliable biochemical marker for screening 21-hydroxylase deficiency without index persons among hirsute women in agreement with HLA haplotyping
20. Clinical and biological phenotypes in late onset 21-hydroxylase deficiency
21. ACTH stimulation test and plasma dehydroepiandrosterone sulfate levels in women with hirsutism
22. Stress induced inhibition of the hypothalamic-pituitary-thyroid axes is attenuated in the aged Fisher 3NN/N male rat
23. Effects of chronic immobilization stress on GH and TSH secretion in the rat: Response to hypothalamic regulatory factors
24. Pulsatile thyrotropin secretion in patients with Addison's disease during variable glucocorticoid therapy
25. Acute changes in serum thyrotropin in treated Addison's disease
26. Changes in adrenal status affect hypothalamic thyrotropin-releasing hormone gene expression in parallel with corticotropin-releasing hormone
27. Involvement of corticotropin-releasing factor and somatostatin in stress-induced inhibition of growth hormone secretion in the rat
28. Environment, human reproduction, menopause and andropause
29. Dynamics of 24-hour pulsatile cortisol, 7-hydroxyprogesterone and androstenedione release in prepubertal patients with nonclassic 21-hydroxylase deficiency and normal prepubertal children