先天性肾上腺增生
男性化
医学
多学科团队
多学科方法
性发育障碍
醛固酮
核型
儿科
内分泌学
内科学
染色体
激素
护理部
遗传学
雄激素
社会学
基因
生物
社会科学
作者
Noor Zwayne,Reeti Chawla,Kathleen van Leeuwen
标识
DOI:10.1097/aog.0000000000005263
摘要
Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder affecting cortisol and aldosterone biosynthesis, which can lead to virilization in fetuses with a 46,XX karyotype. 21-hydroxylase deficiency is the most common cause of CAH, accounting for 90-99% of all patients with the condition. The management of patients with CAH should be done with a multidisciplinary team, which would address all of the complex components of their care throughout their lifespans. Many multidisciplinary teams have adopted shared decision-making approaches to genital surgery in which parents and patients can be part of the decision-making process. Continued research is needed to best serve these patients throughout their lifespans.
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