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本文报道9例婴儿CAH生长发育前瞻性研究和血浆肾上腺类固醇浓度的变化。 病人和方法 9例出生后不久即诊断的CAH,7例典型失盐型21羟化酶缺陷,根据治疗前血浆17羟孕酮(17OHP)升高而诊断;2例11β羟化酶缺陷,根据血浆11-去氧考的松和其尿内代谢产物四氢-11-去氧考的松分泌增加而诊断。6例洽疗前测血浆睾
This article reports 9 cases of infant CAH growth and development of prospective studies and changes in plasma adrenal steroid concentrations. PATIENTS AND METHODS Nine patients with CAH diagnosed shortly after birth and seven patients with typical loss-of-salt 21-hydroxylase deficiency were diagnosed according to a rise in pre-treatment plasma 17-OHP; two cases of 11-beta hydroxylase deficiency were identified according to Plasma 11-deoxy-pine and its urinary metabolites tetrahydro-11-deoxy-pineopsis secretion increased diagnosis. 6 cases of plasma testosterone before treatment