BIOMAT Database Logo BIOMAT Database Logo

[Familial male pseudohermaphroditism due to a testicular 17 ketosteroid reductase defect (author's transl)]. 1973

J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet

UI MeSH Term Description Entries
D007985 Leydig Cells Steroid-producing cells in the interstitial tissue of the TESTIS. They are under the regulation of PITUITARY HORMONES; LUTEINIZING HORMONE; or interstitial cell-stimulating hormone. TESTOSTERONE is the major androgen (ANDROGENS) produced. Interstitial Cells, Testicular,Leydig Cell,Testicular Interstitial Cell,Testicular Interstitial Cells,Cell, Leydig,Cell, Testicular Interstitial,Cells, Leydig,Cells, Testicular Interstitial,Interstitial Cell, Testicular
D007986 Luteinizing Hormone A major gonadotropin secreted by the adenohypophysis (PITUITARY GLAND, ANTERIOR). Luteinizing hormone regulates steroid production by the interstitial cells of the TESTIS and the OVARY. The preovulatory LUTEINIZING HORMONE surge in females induces OVULATION, and subsequent LUTEINIZATION of the follicle. LUTEINIZING HORMONE consists of two noncovalently linked subunits, alpha and beta. Within a species, the alpha subunit is common in the three pituitary glycoprotein hormones (TSH, LH and FSH), but the beta subunit is unique and confers its biological specificity. ICSH (Interstitial Cell Stimulating Hormone),Interstitial Cell-Stimulating Hormone,LH (Luteinizing Hormone),Lutropin,Luteoziman,Luteozyman,Hormone, Interstitial Cell-Stimulating,Hormone, Luteinizing,Interstitial Cell Stimulating Hormone
D008297 Male Males
D010088 Oxidoreductases The class of all enzymes catalyzing oxidoreduction reactions. The substrate that is oxidized is regarded as a hydrogen donor. The systematic name is based on donor:acceptor oxidoreductase. The recommended name will be dehydrogenase, wherever this is possible; as an alternative, reductase can be used. Oxidase is only used in cases where O2 is the acceptor. (Enzyme Nomenclature, 1992, p9) Dehydrogenases,Oxidases,Oxidoreductase,Reductases,Dehydrogenase,Oxidase,Reductase
D004958 Estradiol The 17-beta-isomer of estradiol, an aromatized C18 steroid with hydroxyl group at 3-beta- and 17-beta-position. Estradiol-17-beta is the most potent form of mammalian estrogenic steroids. 17 beta-Estradiol,Estradiol-17 beta,Oestradiol,17 beta-Oestradiol,Aerodiol,Delestrogen,Estrace,Estraderm TTS,Estradiol Anhydrous,Estradiol Hemihydrate,Estradiol Hemihydrate, (17 alpha)-Isomer,Estradiol Monohydrate,Estradiol Valerate,Estradiol Valeriante,Estradiol, (+-)-Isomer,Estradiol, (-)-Isomer,Estradiol, (16 alpha,17 alpha)-Isomer,Estradiol, (16 alpha,17 beta)-Isomer,Estradiol, (17-alpha)-Isomer,Estradiol, (8 alpha,17 beta)-(+-)-Isomer,Estradiol, (8 alpha,17 beta)-Isomer,Estradiol, (9 beta,17 alpha)-Isomer,Estradiol, (9 beta,17 beta)-Isomer,Estradiol, Monosodium Salt,Estradiol, Sodium Salt,Estradiol-17 alpha,Estradiol-17beta,Ovocyclin,Progynon-Depot,Progynova,Vivelle,17 beta Estradiol,17 beta Oestradiol,Estradiol 17 alpha,Estradiol 17 beta,Estradiol 17beta,Progynon Depot
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012734 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. Disorders of Sexual Development,Sex Development Disorders,Sex Differentiation Disorders,Ambiguous Genitalia,Genital Ambiguity,Hermaphroditism,Intersex Conditions,Intersexuality,Pseudohermaphroditism,Sexual Development Disorders,Sexual Differentiation Disorders,Ambiguities, Genital,Ambiguity, Genital,Condition, Intersex,Conditions, Intersex,Differentiation Disorder, Sex,Differentiation Disorder, Sexual,Differentiation Disorders, Sex,Differentiation Disorders, Sexual,Disorder, Sex Differentiation,Disorder, Sexual Differentiation,Disorders, Sex Differentiation,Disorders, Sexual Differentiation,Genital Ambiguities,Genitalia, Ambiguous,Intersex Condition,Intersexualities,Sex Development Disorder,Sex Differentiation Disorder,Sexual Development Disorder,Sexual Differentiation Disorder
D013737 Testis The male gonad containing two functional parts: the SEMINIFEROUS TUBULES for the production and transport of male germ cells (SPERMATOGENESIS) and the interstitial compartment containing LEYDIG CELLS that produce ANDROGENS. Testicles,Testes,Testicle
D015068 17-Ketosteroids Steroids that contain a ketone group at position 17. 17-Oxosteroids,17 Ketosteroids,17 Oxosteroids

Related Publications

J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
Male pseudohermaphroditism due to testicular 17-ketosteroid reductase deficiency.
July 1976, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme,
J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
Familial male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect. I. Studies in vivo.
May 1971, The Journal of clinical endocrinology and metabolism,
J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
Familial male pseudohermaphroditism without gynecomastia due to deficient testicular 17-ketosteroid reductase activity.
October 1974, The New England journal of medicine,
J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
Male pseudohermaphroditism due to deficiency of testicular 17-ketosteroid reductase.
March 1983, Acta paediatrica Scandinavica,
J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
Male pseudohermaphroditism with gynaecomastia due to testicular 17-ketosteroid reductase deficiency.
December 1977, Clinical endocrinology,
J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
[Study of a new case of male pseudohermaphroditism due to 17-ketosteroid reductase deficiency (author's transl)].
January 1979, Annales d'endocrinologie,
J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
Further in vivo studies in male pseudohermaphroditism with gynecomastia due to a testicular 17-ketosteroid reductase defect (compared to a case of testicular feminization).
March 1972, The Journal of clinical endocrinology and metabolism,
J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
[Proceedings: Male pseudohermaphroditism due to testicular 17 beta hydroxysteroid deshydrogenase deficiency (author's transl)].
January 1975, Annales d'endocrinologie,
J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
Testicular 17-ketosteroid reductase deficiency as a cause of male pseudohermaphroditism in 2 sibs.
January 1975, Birth defects original article series,
J Tourniaire, and B Laubie, and J Saez, and T K Leung, and J Perrin, and N Dutrieux, and P Guinet
[Familial case of male pseudohermaphroditism due to 17-ketoreductase defect: late diagnosis in the "aunt" of a patient with the same defect (author's transl)].
January 1979, Annales d'endocrinologie,
Copied contents to your clipboard!