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Replacement oral ethinyloestradiol therapy for gonadal dysgenesis: growth and adrenal androgen studies.
Acta Endocrinol (Copenh) ; 91(3): 519-28, 1979 Jul.
Article in En | MEDLINE | ID: mdl-224633
ABSTRACT
We have studied growth and adrenal dehydroepiandrosterone (DHA) responses to iv synthetic adrenocorticotrophic hormone (ACTH, Cortrosyn) in 6 girls with gonadal dysgenesis before and during treatment with low-dose ethinyloestradiol (EOe2). In all patients there was a statisfactory induction of secondary sexual characteristics including increase in breasts and public hair and onset of withdrawal bleeding within 6 months of therapy. Height velocity increased from 2.8 +/- 0.9 cm/year pre-treatment to 5.3 +/- 1.5 cm/year (P less than 0.02) in the first year. There was deceleration to 1.9 +/- 1.1 cm/year in the second year. There was no disproportionate advancement in bone age and thus, presumably, no loss of ultimate height. We could demonstrate no change in basal or ACTH-stimulated levels of DHA, a specific adrenal androgen, to account for the increased public hair and growth in these patients.
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Collection: 01-internacional Database: MEDLINE Main subject: Turner Syndrome / Dehydroepiandrosterone / Adrenocorticotropic Hormone / Ethinyl Estradiol Limits: Adolescent / Female / Humans Language: En Journal: Acta Endocrinol (Copenh) Year: 1979 Document type: Article
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Collection: 01-internacional Database: MEDLINE Main subject: Turner Syndrome / Dehydroepiandrosterone / Adrenocorticotropic Hormone / Ethinyl Estradiol Limits: Adolescent / Female / Humans Language: En Journal: Acta Endocrinol (Copenh) Year: 1979 Document type: Article
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