17-alpha-hydroxyprogesterone has been researched along with Ambiguous Genitalia in 22 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (18.18) | 18.7374 |
1990's | 7 (31.82) | 18.2507 |
2000's | 5 (22.73) | 29.6817 |
2010's | 6 (27.27) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
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Chan, AO; Hui, E; Lam, KS; Lang, BH; Lee, AC; Tan, KC | 1 |
Ariani, MD; Bruggenwirth, HT; de Jong, FH; Drop, SL; Eggers, S; Faradz, SM; Hersmus, R; Juniarto, AZ; Looijenga, LH; Santosa, A; Sinclair, A; Themmen, AP; van der Zwan, YG; White, SJ; Wolffenbuttel, KP | 1 |
Auchus, RJ; Chang, AY | 1 |
Ahmed, SF; Rodie, M | 1 |
de Jong, FH; Drop, SL; Faradz, SM; Goossens, K; Juniarto, AZ; Setyawati, BA | 1 |
Balogh, E; Jakab, J; Kiss, A; Kovács, J; Ladányi, E; Megyeri, T; Papp, J; Ságodi, L; Ujfalusi, A | 1 |
Elmay, M; Kacem, M; Kacem, SB; Mahjoub, S; Said, M; Youssef, FH | 1 |
DECECCO, C; LOJODICE, G; VENTO, R | 1 |
Cobbaert, C; de Jong, FH; Koper, JW; ten Kate-Booij, MJ | 1 |
Balouch, IL; Bhanji, R; Billoo, AG; Khan, AH; Nazir, Z; Sabir, S | 1 |
Listernick, R; Silverman, BL | 1 |
Conte, FA; Fisher, CR; Grumbach, MM; Ito, Y; Simpson, ER | 1 |
Al-Alwan, I; Daneman, A; Daneman, D; Navarro, O | 1 |
Fujieda, K; Kouda, N; Miller, WL; Nakae, J; Tajima, T | 1 |
Engels, H; Kempe, A; Meindl, A; Plath, H; Rhiem, K; Schmutzler, RK; Schubert, R; Schwanitz, G; van der Ven, K | 1 |
McGillivray, BC | 1 |
Augarten, A; Chayen, R; Gazit, E; Goldfarb, H; Pariente, C; Sack, J | 1 |
Besser, GM; Kirby, RS; Kirk, JM; Perry, LA; Savage, MO; Shand, WS | 1 |
Job, JC; Leymarie, P; Nahoul, K; Perrin, C | 1 |
Dauvergne, M; Forest, MG; Nivelon, JL; Nivelon-Chevallier, A; Tenenbaum, D; Turc, C | 1 |
Ashkenazy, M; Barash, A; Borenstein, R; Coslovsky, R; Lancet, M | 1 |
4 review(s) available for 17-alpha-hydroxyprogesterone and Ambiguous Genitalia
Article | Year |
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46,XX DSD: the masculinised female.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Glands; Adrenal Hyperplasia, Congenital; Adult; Antley-Bixler Syndrome Phenotype; Child; Cosyntropin; Dehydroepiandrosterone; Dihydrotestosterone; Disorders of Sex Development; Female; Gonadal Dysgenesis, 46,XX; Humans; Infant, Newborn; Sex Differentiation; Steroid 11-beta-Hydroxylase; Steroid 21-Hydroxylase; Steroids; Virilism | 2010 |
Investigation and initial management of ambiguous genitalia.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Hyperplasia, Congenital; Anti-Mullerian Hormone; Child; Child, Preschool; Chorionic Gonadotropin; Disorders of Sex Development; Female; Genitalia; Humans; Infant; Infant, Newborn; Male; Parents; Patient Care Team; Progesterone Reductase; Steroid 11-beta-Hydroxylase; Steroid 17-alpha-Hydroxylase; Steroid 21-Hydroxylase; Testosterone | 2010 |
The newborn with ambiguous genitalia.
Topics: 17-alpha-Hydroxyprogesterone; Disorders of Sex Development; Female; Gender Identity; Genitalia; Humans; Hydroxyprogesterones; Infant, Newborn; Karyotyping; Male; Urologic Diseases | 1992 |
Female pseudohermaphroditism due to a maternal adrenocortical tumor.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Gland Neoplasms; Adult; Androgens; Disorders of Sex Development; Female; Humans; Hydroxyprogesterones; Male; Maternal-Fetal Exchange; Paraneoplastic Endocrine Syndromes; Pregnancy; Pregnancy Complications, Neoplastic | 1990 |
18 other study(ies) available for 17-alpha-hydroxyprogesterone and Ambiguous Genitalia
Article | Year |
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Congenital adrenal hyperplasia presenting as a large adrenal incidentaloma in an elderly man.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Gland Neoplasms; Adrenal Glands; Adrenal Hyperplasia, Congenital; Adrenalectomy; Aged; Disorders of Sex Development; Estradiol; Gonadal Steroid Hormones; Humans; Incidental Findings; Karyotype; Male; Phenotype; Salpingo-oophorectomy; Scrotum; Tomography Scanners, X-Ray Computed | 2017 |
Hormonal evaluation in relation to phenotype and genotype in 286 patients with a disorder of sex development from Indonesia.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Age Factors; Androstenedione; Child; Child, Preschool; Disorders of Sex Development; Female; Follicle Stimulating Hormone; Genotype; Gonadal Dysgenesis, 46,XY; Hormones; Humans; Indonesia; Infant; Infant, Newborn; Luteinizing Hormone; Male; Phenotype; Sex Chromosomes; Testosterone | 2016 |
Correlation between androstenedione and 17-hydroxyprogesterone levels in the saliva and plasma of patients with congenital adrenal hyperplasia.
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Adrenal Hyperplasia, Congenital; Androstenedione; Child; Child, Preschool; Disorders of Sex Development; Dose-Response Relationship, Drug; Female; Glucocorticoids; Humans; Hydrocortisone; Infant; Plasma; Saliva; Time Factors | 2011 |
[Dysgenetic male pseudohermaphroditism].
Topics: 17-alpha-Hydroxyprogesterone; Androstenedione; Biomarkers; Chromosomes, Human, X; Chromosomes, Human, Y; Diagnosis, Differential; Disorder of Sex Development, 46,XY; Disorders of Sex Development; Follicle Stimulating Hormone; Humans; Hypospadias; In Situ Hybridization, Fluorescence; Infant, Newborn; Luteinizing Hormone; Male; Mosaicism; Testis; Testosterone | 2012 |
[Feminine pseudo-hermaphroditism and ovarian polycystic syndrome: the role of hydrocortisone].
Topics: 17-alpha-Hydroxyprogesterone; Adolescent; Breast; Disorders of Sex Development; Female; Follicle Stimulating Hormone; Gonadal Steroid Hormones; Humans; Hydrocortisone; Luteinizing Hormone; Menarche; Polycystic Ovary Syndrome; Testosterone; Ultrasonography | 2002 |
[FEMALE PSEUDOHERMAPHRODITISM PROBABLY INDUCED BY A PROGESTINIC ADMINISTERED INTRAMUSCULARLY: 17-ALPHA-HYDROXYPROGESTERONE CAPRONATE].
Topics: 17 alpha-Hydroxyprogesterone Caproate; 17-alpha-Hydroxyprogesterone; 46, XX Disorders of Sex Development; Abnormalities, Drug-Induced; Abortion, Threatened; Disorders of Sex Development; Female; Humans; Hydroxyprogesterones; Infant; Infant, Newborn; Pregnancy; Progestins; Toxicology | 1964 |
Deficiency of 17,20-lyase causing giant ovarian cysts in a girl and a female phenotype in her 46,XY sister: case report.
Topics: 17-alpha-Hydroxyprogesterone; Abdominal Pain; Adolescent; Alleles; Androstenedione; Dehydroepiandrosterone; Disorders of Sex Development; Estrogens; Exons; Female; Follicle Stimulating Hormone; Gene Deletion; Heterozygote; Humans; Luteinizing Hormone; Male; Mutation; Ovarian Cysts; Phenotype; Progesterone; Steroid 17-alpha-Hydroxylase | 2004 |
Profile of children with congenital adrenal hyperplasia--a hospital study.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Child; Child, Preschool; Disorders of Sex Development; Female; Humans; Infant; Infant, Newborn; Male; Pakistan; Retrospective Studies; Risk Factors; Virilism | 2004 |
Cardiomyopathy with congenital adrenal hyperplasia.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Cardiomyopathies; Disorders of Sex Development; Humans; Hydroxyprogesterones; Infant, Newborn; Male | 1994 |
A syndrome of female pseudohermaphrodism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450arom).
Topics: 17-alpha-Hydroxypregnenolone; 17-alpha-Hydroxyprogesterone; Adolescent; Adrenocorticotropic Hormone; Androgens; Aromatase; Cortodoxone; Disorders of Sex Development; Estradiol; Female; Follicle Stimulating Hormone; Gonadotropin-Releasing Hormone; Humans; Hydroxyprogesterones; Hypogonadism; Luteinizing Hormone; Ovary; Point Mutation; Polycystic Ovary Syndrome; Syndrome | 1994 |
Clinical utility of adrenal ultrasonography in the diagnosis of congenital adrenal hyperplasia.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Child; Child, Preschool; Diagnosis, Differential; Disorders of Sex Development; Female; Fetal Diseases; Glucocorticoids; Humans; Infant; Infant, Newborn; Male; Pregnancy; Retrospective Studies; Sensitivity and Specificity; Ultrasonography; Water-Electrolyte Imbalance | 1999 |
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; Amino Acid Sequence; Base Sequence; Cholesterol Side-Chain Cleavage Enzyme; Corticosterone; Dehydroepiandrosterone Sulfate; Disorders of Sex Development; Exons; Female; Heterozygote; Humans; Hydrocortisone; Infant; Introns; Male; Molecular Sequence Data; Pedigree; Renin | 2001 |
Familial ovarian dysgerminomas (Swyer syndrome) in females associated with 46 XY-karyotype.
Topics: 17-alpha-Hydroxyprogesterone; Adult; Androstenedione; Chromosomes, Human, Pair 9; Chromosomes, Human, X; Dihydrotestosterone; Disorders of Sex Development; DNA Mutational Analysis; Estradiol; Female; Follicle Stimulating Hormone; Genitalia; Gonadal Dysgenesis, 46,XY; Humans; In Situ Hybridization, Fluorescence; Karyotyping; Luteinizing Hormone; Male; Ovarian Neoplasms; Pedigree; Phenotype; Progesterone; Prolactin; Reference Values; Sequence Analysis, DNA; Sex Chromosomes; Testosterone; Ultrasonography; Uterus | 2002 |
Ambiguous genitalia due to partial activity of cytochromes P450c17 and P450c21.
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Androstenedione; Chorionic Gonadotropin; Chromosomes, Human, Pair 10; Chromosomes, Human, Pair 6; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Disorders of Sex Development; Female; Histocompatibility Testing; Humans; Hydrocortisone; Hydroxyprogesterones; Infant; Male; Mutation; Pedigree; Progesterone; Sincalide; Testosterone | 1992 |
Boy or girl?
Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Antibody Specificity; Disorders of Sex Development; Humans; Hydroxyprogesterones; Infant, Newborn; Reagent Kits, Diagnostic | 1991 |
[Elevated levels of plasma 4-ene steroids in a case of congenital deficiency of 3 beta-hydroxysteroid dehydrogenase].
Topics: 17-alpha-Hydroxypregnenolone; 17-alpha-Hydroxyprogesterone; 3-Hydroxysteroid Dehydrogenases; Androstenedione; Dehydroepiandrosterone; Disorders of Sex Development; Humans; Hydrocortisone; Hydroxyprogesterones; Infant; Infant, Newborn; Male; Testosterone | 1989 |
[Prenatal diagnosis in a familial form of male pseudohermaphroditism due to 17-keto reductase deficiency].
Topics: 17-alpha-Hydroxyprogesterone; 17-Hydroxysteroid Dehydrogenases; Amniocentesis; Androstenedione; Chorionic Gonadotropin; Disorders of Sex Development; Humans; Hydroxyprogesterones; Infant, Newborn; Karyotyping; Male; Prenatal Diagnosis; Testosterone | 1985 |
Female pseudohermaphroditism with adrenal cortical tumor in adulthood.
Topics: 17-alpha-Hydroxyprogesterone; Adenoma; Adrenal Cortex Neoplasms; Adult; Age Factors; Cortodoxone; Cosyntropin; Disorders of Sex Development; Female; Humans; Hydrocortisone; Hydroxyprogesterones | 1985 |