Nokoff Natalie J, Buchanan Cindy, Barker Jennifer M
Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Ludeman Family Center for Women's Health Research, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
J Clin Endocrinol Metab. 2025 Jan 21;110(Supplement_1):S13-S24. doi: 10.1210/clinem/dgae563.
The most common form of congenital adrenal hyperplasia (CAH) is secondary to 21-hydroxylase deficiency (21OHD). This review will summarize the clinical manifestations, recommended treatments, monitoring, clinical challenges and management strategy, and treatment challenges in special situations for infants and children with classic CAH due to 21OHD. Specifically, we review newborn screening and the initial diagnosis, glucocorticoid and mineralocorticoid treatment, and recommended monitoring, including anthropometric and laboratory measures. Children with CAH may have premature adrenarche, precocious puberty, and early growth plate closure and have an increased risk of hypertension and overweight/obesity. Many 46,XX individuals will also have genital differences, which may include clitoromegaly and/or a urogenital sinus. We review psychosocial and surgical considerations, including suggestions on how to talk with children, family, and caregivers about bodily difference. These suggestions may be used by families and/or providers caring for individuals with CAH.
先天性肾上腺皮质增生症(CAH)最常见的形式继发于21-羟化酶缺乏症(21OHD)。本综述将总结21OHD所致经典型CAH婴幼儿的临床表现、推荐治疗方法、监测、临床挑战及管理策略,以及特殊情况下的治疗挑战。具体而言,我们将回顾新生儿筛查与初始诊断、糖皮质激素和盐皮质激素治疗,以及推荐的监测,包括人体测量和实验室检查。CAH患儿可能出现肾上腺功能早现、性早熟和生长板过早闭合,且患高血压和超重/肥胖的风险增加。许多46,XX个体还会有生殖器差异,可能包括阴蒂肥大和/或泌尿生殖窦。我们将回顾心理社会和手术方面的考虑因素,包括关于如何与儿童、家庭和护理人员谈论身体差异的建议。这些建议可供照顾CAH患者的家庭和/或医疗人员使用。