Page last updated: 2024-08-17

androstenedione and 46, XY Gonadal Dysgenesis

androstenedione has been researched along with 46, XY Gonadal Dysgenesis in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (28.57)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (14.29)	29.6817
2010's	4 (57.14)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Afeltra, L; Alviggi, C; Cariati, F; Colao, A; Di Somma, C; Galdiero, M; Lo Calzo, F; Melis, D; Pivonello, R; Simeoli, C; Vitale, P	1
Ali, OS; Essawi, ML; Gad, YZ; Hassan, HA; Mazen, I; Mekkawy, M	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
Gu, XF; Han, LS; Liang, LL; Luo, JH; Qiu, WJ; Xu, MS; Ye, J; Yu, YG; Zhang, HW; Zhou, DY	1
Engels, H; Kempe, A; Meindl, A; Plath, H; Rhiem, K; Schmutzler, RK; Schubert, R; Schwanitz, G; van der Ven, K	1
Aono, T; Kinugasa, T; Kurachi, H; Kurachi, K; Matsumoto, K; Takayasu, S	1
Chavez, B; Mendez, JP; Perez-Palacios, G; Saavedra, D; Ulloa-Aguirre, A	1

Reviews

1 review(s) available for androstenedione and 46, XY Gonadal Dysgenesis

Article	Year
The 17β-hydroxysteroid dehydrogenase type 3 deficiency: a case report of an 18-year patient and review of the literature. Minerva endocrinologica, 2013, Volume: 38, Issue:1 Topics: 17-Hydroxysteroid Dehydrogenases; Adolescent; Amenorrhea; Androstenedione; Face; Female; Genitalia; Gonadal Dysgenesis, 46,XY; Hirsutism; Humans; Male; Mutation; Orchiectomy; Phenotype; Testosterone	2013

Other Studies

6 other study(ies) available for androstenedione and 46, XY Gonadal Dysgenesis

Article	Year
A novel nonsense mutation in exon 1 of HSD17B3 gene in an Egyptian 46,XY adult female presenting with primary amenorrhea. Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation, 2013, Volume: 7, Issue:6 Topics: 17-Hydroxysteroid Dehydrogenases; Adult; Amenorrhea; Androstenedione; Base Sequence; Codon, Nonsense; DNA; Egypt; Exons; Female; Gonadal Dysgenesis, 46,XY; Homozygote; Humans; Male; Mutation; Testosterone	2013
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
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
Endocrine and androgen-receptor studies in a patient with XY gonadal agenesis. Obstetrics and gynecology, 1979, Volume: 54, Issue:6 Topics: Adult; Androstenedione; Endocrine Glands; Estradiol; Female; Follicle Stimulating Hormone; Gonadal Dysgenesis; Gonadal Dysgenesis, 46,XY; Gonadotropin-Releasing Hormone; Gonads; Humans; Luteinizing Hormone; Pituitary-Adrenal System; Progesterone; Receptors, Androgen; Receptors, Cell Surface; Receptors, Steroid; Testosterone; Thyroid Gland	1979
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