AnatomyDiseasesChemicals and DrugsAnalytical, Diagnostic and Therapeutic Techniques and EquipmentPsychiatry and PsychologyPhenomena and ProcessesInformation ScienceNamed GroupsHealth Care
Adrenal Hyperplasia, CongenitalSteroid 21-Hydroxylase17-alpha-HydroxyprogesteroneHyperplasiaAdrenal GlandsPregnanetriolFludrocortisoneHydroxyprogesteronesAdrenal Rest TumorAdrenocortical HyperfunctionAdrenal Gland DiseasesVirilismAdrenal InsufficiencyCortodoxone17-KetosteroidsAdrenal CortexAdrenal Gland NeoplasmsAdrenal MedullaMineralocorticoidsHirsutismSteroid 11-beta-HydroxylaseAdrenocorticotropic Hormone17-alpha-HydroxypregnenoloneAntley-Bixler Syndrome PhenotypeProstatic HyperplasiaHydrocortisoneAge Determination by Skeleton46, XY Disorders of Sex DevelopmentCosyntropinEndometrial HyperplasiaNeonatal ScreeningDisorders of Sex DevelopmentAdrenal Cortex NeoplasmsGlucocorticoidsGenetic Diseases, X-LinkedAndrostenedioneDAX-1 Orphan Nuclear ReceptorSexual InfantilismAdrenalectomyPuberty, PrecociousSteroid HydroxylasesGlycerol KinaseReproductive Physiological PhenomenaAndrogensPHEX Phosphate Regulating Neutral EndopeptidaseInfant, NewbornInfant, PostmatureGenitaliaGingival HyperplasiaAdrenal Cortex HormonesObstetric Surgical ProceduresPubertyDexamethasonePrenatal DiagnosisThymus HyperplasiaUrogenital AbnormalitiesFocal Nodular HyperplasiaTestosteroneHypophosphatemiaSteroidsHypophosphatemia, Familial3-Hydroxysteroid DehydrogenasesComplement C4Hormone Replacement TherapyFamilial Hypophosphatemic RicketsMutationHeterozygote DetectionBody HeightPseudogenesCortisoneCushing SyndromePhenotypeTunica IntimaFetal DiseasesTeaching MaterialsAdrenal Cortex DiseasesAdrenocortical AdenomaHeterozygotePregnancyRadioimmunoassayAdrenal Cortex Function TestsRenin
TumorsDeficiencyIncreaseInsufficiencySteroid
Tumors1
  • In males with CAH, 11-oxygenated androgen levels may indicate the presence testicular adrenal rest tumors. (wikipedia.org)
Deficiency1
  • While studies suggest that 11β-OHP, also known as 21-deoxycorticosterone, can be used as marker for adrenal 21-hydroxylase deficiency, another 21-carbon steroid - 21-deoxycortisol (produced from 17α-hydroxyprogesterone) gained acceptance for this purpose. (wikipedia.org)
Increase1
  • 7) The LPS-low group, LPS-mid group, and LPS-high group showed an increase in HYP content and α-SMA expression in the lung tissue of rats. (alljournal.ac.cn)
Insufficiency1
  • It is linked, by an insufficiently described mechanism, to primary adrenal insufficiency (PAI) with or without mineralocorticoid insufficiency and several extra-adrenal manifestations (i.e. gonadal adrenal rest tumors, cardiomyopathy, hypothyroidism, and precocious puberty). (eurospe.org)
Steroid1
  • We tested the hypothesis that multiple alterations in the metabolism of glucocorticoids are required for the development of hypertension in children who become overweight.Methods: Timed spot urine for targeted gas chromatography-mass spectrometry steroid metabolome analysis was collected from (1) overweight/hyp. (eurospe.org)