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Article

Clinical characteristics of a male child with non-classic lipoid congenital adrenal hyperplasia and literature review.

Frontiers in endocrinology - 1 Jan 2022

Lu Wenli, Zhang Tingting, Zhang Lidan, Wang Xueqing, Lv Sheng, Wang Junqi, Ye Lei, Xiao Yuan, Dong Zhiya, Wang Wei, Sun Shuoyue, Li Chuanyin, Hu Ronggui, Ning Guang, Ma Xiaoyu

Abstract excerpt

Background: Lipoid congenital adrenal hyperplasia (LCAH) is a rare and severe disorder that is caused by mutations in the steroidogenic acute regulatory protein (StAR). Non-classic LCAH is defined as late-onset glucocorticoid deficiency and even complete male external genitalia in 46,XY individuals. However, to date, few cases of non-classic LCAH have been reported. Methods: It was attempted to describe the...

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Share to Adrenal Hyperplasia, Congenital
Share to Disorder of Sex Development, 46,XY

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 36407315
DOI: 10.3389/fendo.2022.947762
PMCID: PMC9666400

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