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TREATMENT OF 21-HYDROXYLASE DEFICIENCY IN CONGENITAL (CAH) PATIENTS

TREATMENT OF 21-HYDROXYLASE DEFICIENCY IN CONGENITAL (CAH) PATIENTS
先天性 (CAH) 患者 21-羟化酶缺乏症的治疗
批准号：
3884678
负责人：
DOROTHY J. BECKER
金额：
$0.0万
依托单位：
CHILDREN'S HOSP PITTSBURGH/UPMC HLTH SYS
依托单位国家：
美国
项目类别：
财政年份：
--
资助国家：
美国
项目状态：
未结题
起止时间：
至
来源：
https://reporter.nih.gov/project-details/3884678
关键词：
adrenal hyperplasia adrenocorticotropic hormone congenital disorders endocrine disorder diagnosis human subject human therapy evaluation pediatrics

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英文摘要
Hormonal profiles before and after ACTH stimulation, with patient signs and symptoms, are compared with those in normal individuals to define abnormal responses and make the diagnosis of mild defects possible. Need and effectiveness of treatment is assessed by measuring hormones at specific times after the administration of medication.
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