Compounds > 17-alpha-hydroxyprogesterone
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17-alpha-hydroxyprogesterone and Abnormalities, Multiple

17-alpha-hydroxyprogesterone has been researched along with Abnormalities, Multiple in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hartmann, MF; Holterhus, PM; Reinehr, T; Rothermel, J; Wegener-Panzer, A; Wudy, SA1
Bahíllo-Curieses, MP; del Cañizo López, A; Loidi Fernández de Trocóniz, L; Martínez-Sopena, MJ1
Biason-Lauber, A; Gueorguieva, I; Lebon-Labich, B; Paris, F; Philibert, P; Pienkowski, C; Stuckens, C; Sultan, C1
Cragun, DL; Hopkin, RJ; Kelley, RI; Leslie, ND; Mulrooney, NP; Shackleton, CH; Trumpy, SK1
Arlt, W; Draper, N; Hartmann, MF; Stewart, PM; Wudy, SA1

Other Studies

5 other study(ies) available for 17-alpha-hydroxyprogesterone and Abnormalities, Multiple

ArticleYear
Vanishing 17-Hydroxyprogesterone Concentrations in 21-Hydroxylase Deficiency.
    Hormone research in paediatrics, 2018, Volume: 90, Issue:2

    Topics: 17-alpha-Hydroxyprogesterone; Abnormalities, Multiple; Adrenal Cortex Diseases; Adrenal Hyperplasia, Congenital; Adrenal Insufficiency; Aftercare; Child; Child, Preschool; Delayed Diagnosis; Humans; Hydrocortisone; Infant; Infant, Newborn; Male

2018
[Partial 3ß-hydroxysteroid dehydrogenase type 2 deficiency: Diagnosis of a novel mutation after positive newborn screening for 21-hydroxylase deficiency].
    Medicina clinica, 2016, Jan-15, Volume: 146, Issue:2

    Topics: 17-alpha-Hydroxyprogesterone; Abnormalities, Multiple; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Chorionic Gonadotropin; Diagnostic Errors; Disorder of Sex Development, 46,XY; Heterozygote; Hormones; Humans; Infant, Newborn; Male; Mutation, Missense; Neonatal Screening; Point Mutation; Progesterone Reductase; Testis; Testosterone

2016
Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome).
    Fertility and sterility, 2011, Jun-30, Volume: 95, Issue:8

    Topics: 17-alpha-Hydroxyprogesterone; 46, XX Disorders of Sex Development; Abnormalities, Multiple; Adolescent; Androstenedione; beta Catenin; Cell Line, Tumor; Congenital Abnormalities; Dehydroepiandrosterone; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Heterozygote; Humans; Hyperandrogenism; Kidney; Mullerian Ducts; Mutation; Ovary; Phenotype; Progesterone Reductase; RNA, Messenger; Somites; Spine; Steroid 17-alpha-Hydroxylase; Transfection; Uterus; Vagina; Wnt Proteins; Wnt4 Protein; Young Adult

2011
Undetectable maternal serum uE3 and postnatal abnormal sterol and steroid metabolism in Antley-Bixler syndrome.
    American journal of medical genetics. Part A, 2004, Aug-15, Volume: 129A, Issue:1

    Topics: 17-alpha-Hydroxyprogesterone; Abnormalities, Multiple; Adult; Child, Preschool; Craniosynostoses; Estriol; Face; Fatal Outcome; Female; Genitalia; Humans; Infant; Infant, Newborn; Karyotyping; Male; Pregnancy; Pregnancy Trimester, Third; Progesterone; Siblings; Steroids; Sterols; Syndrome

2004
A male twin infant with skull deformity and elevated neonatal 17-hydroxyprogesterone: a prismatic case of P450 oxidoreductase deficiency.
    Endocrine research, 2004, Volume: 30, Issue:4

    Topics: 17-alpha-Hydroxyprogesterone; Abnormalities, Multiple; Alanine; Amino Acid Substitution; Cytosine; Diagnosis, Differential; Diseases in Twins; Ear; Female; Guanine; Humans; Infant, Newborn; Male; Marfan Syndrome; NADPH-Ferrihemoprotein Reductase; Proline; Skull; Steroid Metabolism, Inborn Errors; Steroids

2004