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1.
Neuro Endocrinol Lett ; 38(7): 509-518, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29369603

RESUMEN

OBJECTIVE: Lifelong steroid therapy and exposure to adrenal androgen excess in 21-hydroxylase deficient (21-OHD) congenital adrenal hyperplasia (CAH) children and adolescents may modify circadian blood pressure profile and result in vascular complications. The objective of the study was to evaluate vascular abnormalities in 21-OHD children and adolescents in relation to their genotypes. DESIGN: A cross-sectional study conducted at a tertiary referral center. PATIENTS: Seventy patients with 21-OHD CAH (27 boys), aged from 3 to 17.9 years: 9 with nonclassic CAH, 61 with classic CAH: 10 with simple virilising (SV) and 51 with salt wasting CAH (13-Del/Del, 8-Del/I2G, 7-I2G/I2G and 23-other genotypes). MAIN OUTCOMES MEASURES: The assessment of systolic and diastolic BP (SBP, DBP) loads, night dip% and arterial ambulatory stiffness index (AASI) in 21-OHD CAH patients.


Asunto(s)
Hiperplasia Suprarrenal Congénita/fisiopatología , Presión Sanguínea/fisiología , Ritmo Circadiano/fisiología , Genotipo , Rigidez Vascular/fisiología , Adolescente , Hiperplasia Suprarrenal Congénita/sangre , Hiperplasia Suprarrenal Congénita/genética , Presión Sanguínea/genética , Niño , Preescolar , Ritmo Circadiano/genética , Femenino , Humanos , Hidrocortisona/sangre , Masculino , Globulina de Unión a Hormona Sexual/metabolismo , Testosterona/sangre , Rigidez Vascular/genética
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