Compounds > dihydrotestosterone
Page last updated: 2024-08-21

dihydrotestosterone and 46, XY Gonadal Dysgenesis

dihydrotestosterone has been researched along with 46, XY Gonadal Dysgenesis in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19904 (40.00)18.7374
1990's2 (20.00)18.2507
2000's3 (30.00)29.6817
2010's1 (10.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Choi, JH; Kim, GH; Kim, KS; Kim, SH; Seo, EJ; Yoo, HW1
Frankenschmidt, A; Hiort, O; Kienzle, FB; Schwab, KO; Superti-Furga, A; van der Werf-Grohmann, N; Walter, KN; Wudy, SA1
Archer, SM; Dobyns, WB; Innis, JW; Keegan, CE; Lehoczky, J; Mohammed, M; Vilain, E1
David, R; Koo, GC; McMorrow, LE; Roy, S; Wachtel, SS; Wolman, SR1
Glassberg, KI1
Edwards, CR; Hargreaves, TB; Hodgins, MB; Saunders, PT; Simpson, NB; Tincello, DG; Wu, FC1
Engels, H; Kempe, A; Meindl, A; Plath, H; Rhiem, K; Schmutzler, RK; Schubert, R; Schwanitz, G; van der Ven, K1
Angeles, A; Carranza-Lira, S; Chavez, B; Mendez, JP; Perez-Palacios, G; Ulloa-Aguirre, A1
Chavez, B; Mendez, JP; Perez-Palacios, G; Saavedra, D; Ulloa-Aguirre, A1
Kulin, HE; Monsaert, RP; Stumpf, PG; Wachtel, SS; Warner, BA1

Other Studies

10 other study(ies) available for dihydrotestosterone and 46, XY Gonadal Dysgenesis

ArticleYear
Molecular analysis of the AR and SRD5A2 genes in patients with 46,XY disorders of sex development.
    Journal of pediatric endocrinology & metabolism : JPEM, 2008, Volume: 21, Issue:6

    Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Adolescent; Child; Child, Preschool; Dihydrotestosterone; DNA Mutational Analysis; Early Diagnosis; Female; Follicle Stimulating Hormone; Genetic Testing; Gonadal Dysgenesis, 46,XY; Humans; Infant; Infant, Newborn; Luteinizing Hormone; Male; Receptors, Androgen; Testosterone

2008
Difficulties in diagnosis and treatment of 5alpha-reductase type 2 deficiency in a newborn with 46,XY DSD.
    Hormone research in paediatrics, 2010, Volume: 74, Issue:1

    Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Dihydrotestosterone; Female; Gonadal Dysgenesis, 46,XY; Humans; Infant, Newborn; Male; Point Mutation; Testosterone

2010
Microcephaly, jejunal atresia, aberrant right bronchus, ocular anomalies, and XY sex reversal.
    American journal of medical genetics. Part A, 2004, Mar-15, Volume: 125A, Issue:3

    Topics: Abnormalities, Multiple; Bronchi; Digestive System Abnormalities; Dihydrotestosterone; Disorders of Sex Development; Eye Abnormalities; Gene Dosage; Gonadal Dysgenesis, 46,XY; Humans; Infant; Intestinal Atresia; Jejunum; Male; Microcephaly; Nucleic Acid Hybridization; Polymerase Chain Reaction; Receptors, Androgen; Testis; Testosterone

2004
Aberrant testicular differentiation in 46,XY gonadal dysgenesis: morphology, endocrinology, serology.
    Human genetics, 1980, Volume: 55, Issue:3

    Topics: Cells, Cultured; Dihydrotestosterone; Gonadal Dysgenesis; Gonadal Dysgenesis, 46,XY; Gonads; H-Y Antigen; Humans; Infant, Newborn; Lung; Male; Testosterone

1980
Gender assignment in newborn male pseudohermaphrodites.
    The Urologic clinics of North America, 1980, Volume: 7, Issue:2

    Topics: 3-Oxo-5-alpha-Steroid 4-Dehydrogenase; Androgen-Insensitivity Syndrome; Dihydrotestosterone; Disorders of Sex Development; Gonadal Dysgenesis, 46,XY; Gonadal Dysgenesis, Mixed; Humans; Infant, Newborn; Male; Mullerian Ducts; Sex Determination Analysis; Syndrome; Testosterone; Ultrasonography

1980
Correlation of clinical, endocrine and molecular abnormalities with in vivo responses to high-dose testosterone in patients with partial androgen insensitivity syndrome.
    Clinical endocrinology, 1997, Volume: 46, Issue:4

    Topics: Adult; Androgens; Dihydrotestosterone; Disorders of Sex Development; DNA; Drug Administration Schedule; Electrophoresis; Estradiol; Follicle Stimulating Hormone; Gonadal Dysgenesis, 46,XY; Humans; Luteinizing Hormone; Male; Nitrogen; Receptors, Androgen; Sebum; Sex Hormone-Binding Globulin; Testosterone

1997
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
Incomplete regression of müllerian ducts in the androgen insensitivity syndrome.
    Fertility and sterility, 1990, Volume: 53, Issue:6

    Topics: Adolescent; Androgens; Animals; Child; Dihydrotestosterone; Fallopian Tubes; Female; Follicle Stimulating Hormone; Gonadal Dysgenesis; Gonadal Dysgenesis, 46,XY; Humans; Luteinizing Hormone; Male; Mullerian Ducts; Nandrolone; Receptors, Androgen; Testis

1990
Inherited impairment of nuclear androgen uptake as a cause of familial androgen insensitivity.
    European journal of obstetrics, gynecology, and reproductive biology, 1988, Volume: 28, Issue:4

    Topics: Androgens; Androstenedione; Child; Chorionic Gonadotropin; Dihydrotestosterone; Disorders of Sex Development; Follicle Stimulating Hormone; Gonadal Dysgenesis; Gonadal Dysgenesis, 46,XY; Humans; Infant; Luteinizing Hormone; Male; Pedigree; Receptors, Androgen; Syndrome; Testosterone

1988
46,XY gonadal dysgenesis: is oncogenesis related to H-Y phenotype or breast development?
    Human genetics, 1985, Volume: 69, Issue:1

    Topics: Adolescent; Adult; Breast; Cell Transformation, Neoplastic; Child; Dihydrotestosterone; Dysgerminoma; Estradiol; Estrone; Female; Gonadal Dysgenesis; Gonadal Dysgenesis, 46,XY; H-Y Antigen; Humans; Hydrocortisone; Ovarian Neoplasms; Phenotype; Prolactin; Testosterone

1985