corticosterone has been researched along with Disorders of Sex Development in 17 studies
Disorders of Sex Development: In gonochoristic organisms, congenital conditions in which development of chromosomal, gonadal, or anatomical sex is atypical. Effects from exposure to abnormal levels of GONADAL HORMONES in the maternal environment, or disruption of the function of those hormones by ENDOCRINE DISRUPTORS are included.
Excerpt | Relevance | Reference |
---|---|---|
"A case of male pseudohermaphroditism associated with 17 alpha-hydroxylase deficiency is reported in which the diagnosis was firmly established by gas chromatography-mass spectrometry." | 1.27 | Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency: diagnosis by gas chromatography--mass spectrometry. ( Betz, G; Burstein, P; Fennessey, P; Marsh, P, 1983) |
"The male pseudohermaphroditism resulted from deficient testosterone synthesis due to deficiency of 17 alpha-hydroxylase and 17,20 desmolase." | 1.27 | Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia. ( Gautier, T; Imperato-McGinley, J; Peterson, RE; Shackleton, C, 1985) |
"Corticosterone levels were 70 and 92 ng/ml and rose after ACTH (110 and 180 ng/ml)." | 1.26 | Dexamethasone-suppressible hypercorticosteronism in two 46,XX subjects with ambiguous genitalia and ovarian cysts. Partial defect of 17 alpha-hydroxylase or 17-20-desmolase. ( Canlorbe, P; Dehennin, L; Girard, F; Konopka, P; Merceron, RE; Roger, M; Seneze, J; Toublanc, JE, 1982) |
"A case of male pseudohermaphroditism aged 48 years with systemic hypertension and hypokalaemic alkalosis is described." | 1.26 | Male pseudohermaphroditism with hypertension due to a 17alpha-hydroxylation deficiency. ( Audi-Parera, L; Blum, J; Castelnovo, P; Forest, MG; Loras, B; Tourniaire, J, 1976) |
"Pregnancy was not maintained; however, after 22 days, resorption sites were still visable." | 1.25 | Biological profile of quingestanol acetate. ( Giannina, T; McDougall, EA; Meli, A; Rassaert, CL; Steinetz, BG, 1969) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 15 (88.24) | 18.7374 |
1990's | 1 (5.88) | 18.2507 |
2000's | 1 (5.88) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
COLE, VW | 1 |
MIN, BS | 1 |
KAWATE, R | 1 |
ROSE, RG | 1 |
HOWE, CD | 1 |
Roger, M | 1 |
Merceron, RE | 1 |
Girard, F | 1 |
Canlorbe, P | 1 |
Dehennin, L | 1 |
Konopka, P | 1 |
Seneze, J | 1 |
Toublanc, JE | 1 |
Burstein, P | 1 |
Marsh, P | 1 |
Fennessey, P | 1 |
Betz, G | 1 |
Tajima, T | 1 |
Fujieda, K | 1 |
Kouda, N | 1 |
Nakae, J | 1 |
Miller, WL | 1 |
Tourniaire, J | 1 |
Audi-Parera, L | 1 |
Loras, B | 1 |
Blum, J | 1 |
Castelnovo, P | 1 |
Forest, MG | 1 |
Biglieri, EG | 1 |
Waldhäusl, W | 1 |
Herkner, K | 1 |
Nowotny, P | 1 |
Bratusch-Marrain, P | 1 |
Horton, R | 1 |
Imperato-McGinley, J | 4 |
Shackleton, C | 4 |
Orlic, S | 1 |
Stoner, E | 1 |
Peterson, RE | 3 |
Gautier, T | 3 |
Arthur, A | 1 |
Parks, GA | 1 |
Dumars, KW | 1 |
Limbeck, GA | 1 |
Quinlivan, WL | 1 |
New, MI | 1 |
Hammerstein, J | 1 |
Zielske, F | 1 |
Dsitler, A | 1 |
Wolff, HP | 1 |
Goldman, AS | 1 |
Gustafsson, JA | 1 |
Gustafsson, SA | 1 |
Bricaire, H | 1 |
Luton, JP | 1 |
Laudat, P | 1 |
Legrand, JC | 1 |
Turpin, G | 1 |
Corvol, P | 1 |
Lemmer, M | 1 |
Giannina, T | 1 |
Steinetz, BG | 1 |
Rassaert, CL | 1 |
McDougall, EA | 1 |
Meli, A | 1 |
1 trial available for corticosterone and Disorders of Sex Development
Article | Year |
---|---|
C19 and C21 5 beta/5 alpha metabolite ratios in subjects treated with the 5 alpha-reductase inhibitor finasteride: comparison of male pseudohermaphrodites with inherited 5 alpha-reductase deficiency.
Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; 5-alpha Reductase Inhibitors; Aged; Androstenedione; Androste | 1990 |
16 other studies available for corticosterone and Disorders of Sex Development
Article | Year |
---|---|
DIVERSITIES OF ADRENAL CORTICAL HYPERFUNCTION.
Topics: 17-Ketosteroids; Adrenal Gland Neoplasms; Adrenalectomy; Adrenocortical Hyperfunction; Adrenocortico | 1964 |
Dexamethasone-suppressible hypercorticosteronism in two 46,XX subjects with ambiguous genitalia and ovarian cysts. Partial defect of 17 alpha-hydroxylase or 17-20-desmolase.
Topics: Adolescent; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Aldosterone; Corticosteron | 1982 |
Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency: diagnosis by gas chromatography--mass spectrometry.
Topics: Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Adult; Corticosterone; Cross Reactions | 1983 |
Heterozygous mutation in the cholesterol side chain cleavage enzyme (p450scc) gene in a patient with 46,XY sex reversal and adrenal insufficiency.
Topics: 17-alpha-Hydroxyprogesterone; Adrenocortical Hyperfunction; Adrenocorticotropic Hormone; Aldosterone | 2001 |
Male pseudohermaphroditism with hypertension due to a 17alpha-hydroxylation deficiency.
Topics: Acute Kidney Injury; Adrenocorticotropic Hormone; Alkalosis; Androstenedione; Corticosterone; Desoxy | 1976 |
Mechanisms establishing the mineralocorticoid hormone patterns in the 17 alpha-hydroxylase deficiency syndrome.
Topics: 18-Hydroxycorticosterone; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Adult; Aldos | 1979 |
Combined 17 alpha- and 18-hydroxylase deficiency associated with complete male pseudohermaphroditism and hypoaldosteronism.
Topics: Adrenal Hyperplasia, Congenital; Aldosterone; Corticosterone; Desoxycorticosterone; Disorders of Sex | 1978 |
Biosynthetic disorders of the adrenal cortex and gonad.
Topics: Adrenal Cortex; Adrenal Cortex Hormones; Adrenal Glands; Corticosterone; Disorders of Sex Developmen | 1975 |
Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; 18-Hydroxycorticosterone; 18-Hydroxydesoxycorticosterone | 1985 |
Decreased urinary C19 and C21 steroid 5 alpha-metabolites in parents of male pseudohermaphrodites with 5 alpha-reductase deficiency: detection of carriers.
Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Adolescent; Adult; Androstenedione; Androsterone; Chromatogra | 1985 |
Urinary steroid metabolites in subjects with male pseudohermaphroditism due to 5 alpha-reductase deficiency.
Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Adolescent; Adult; Androstenedione; Child; Child, Preschool; | 1985 |
"True agonadism": a misnomer?
Topics: 17-Ketosteroids; Androstenedione; Child, Preschool; Chorionic Gonadotropin; Corticosterone; Dehydroe | 1974 |
17-Alpha-hydroxylase deficiency of the gonads and adrenals in a male pseudohermaphrodite.
Topics: Adolescent; Adrenal Cortex Hormones; Adrenal Glands; Aldosterone; Corticosterone; Culture Techniques | 1973 |
Female pattern of metabolism of (4 14 C)corticosterone in male pseudohermaphroditic rats.
Topics: Animals; Bile; Carbon Isotopes; Chromatography, Gas; Corticosterone; Dimethyl Sulfoxide; Disorders o | 1973 |
A new male pseudo-hermaphroditism associated with hypertension due to a block of 17 -hydroxylation.
Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adult; Aldosterone; Corticosterone; Desoxycorticosterone | 1972 |
Biological profile of quingestanol acetate.
Topics: Adrenal Glands; Androgens; Animals; Body Weight; Corticosterone; Disorders of Sex Development; Estra | 1969 |