Compounds > 17-alpha-hydroxyprogesterone
Page last updated: 2024-08-17

17-alpha-hydroxyprogesterone and 46, XY Gonadal Dysgenesis

17-alpha-hydroxyprogesterone has been researched along with 46, XY Gonadal Dysgenesis in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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, KP1
Gu, XF; Han, LS; Liang, LL; Luo, JH; Qiu, WJ; Xu, MS; Ye, J; Yu, YG; Zhang, HW; Zhou, DY1
Hardoff, R; Luboshitzky, R; Qupti, G; Shen-Orr, Z1
Engels, H; Kempe, A; Meindl, A; Plath, H; Rhiem, K; Schmutzler, RK; Schubert, R; Schwanitz, G; van der Ven, K1

Other Studies

4 other study(ies) available for 17-alpha-hydroxyprogesterone and 46, XY Gonadal Dysgenesis

ArticleYear
Hormonal evaluation in relation to phenotype and genotype in 286 patients with a disorder of sex development from Indonesia.
    Clinical endocrinology, 2016, Volume: 85, Issue:2

    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
[Clinical and genetic analysis of an infant with isolated 17, 20-lyase deficiency].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2016, Volume: 54, Issue:8

    Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Androstenedione; Estradiol; Follicle Stimulating Hormone; Genetic Testing; Gonadal Dysgenesis, 46,XY; High-Throughput Nucleotide Sequencing; Humans; Infant; Luteinizing Hormone; Lyases; Male; Mutation; Progesterone; Steroid 17-alpha-Hydroxylase; Testis; Testosterone

2016
Decreased melatonin secretion in a phenotypically male 46,XX patient with classic 21-hydroxylase deficiency.
    Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association, 2000, Volume: 108, Issue:3

    Topics: 17-alpha-Hydroxyprogesterone; Adrenal Hyperplasia, Congenital; Adult; Dehydroepiandrosterone Sulfate; Dexamethasone; Estradiol; Female; Follicle Stimulating Hormone; Gonadal Dysgenesis, 46,XY; Hormone Replacement Therapy; Humans; Hydrocortisone; Luteinizing Hormone; Male; Melatonin; Oligospermia; Ovariectomy; Testosterone

2000
Familial ovarian dysgerminomas (Swyer syndrome) in females associated with 46 XY-karyotype.
    Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology, 2002, Volume: 16, Issue:2

    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