Case report: Clinical characteristics and Genetical analysis of HSD11B2 in three Chinese children with apparent mineralocorticoid excess: a case series

Case report: Clinical characteristics and Genetical analysis of HSD11B2 in three Chinese children with apparent mineralocorticoid excess: a case series

BackgroundApparent Mineralocorticoid Excess (AME) is a rare autosomal recessive disorder, characterized by a notably complex diagnostic process. To date, the majority of documented cases have been presented as individual case reports. This article aims to enhance the understanding of the course and...

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Bibliographic Details
Main Authors: Yuan Ding, Ming Cheng, Bingyan Cao, Min Liu, Xuyun Hu, Di Wu
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Endocrinology
Subjects:
apparent mineralocorticoid excess
hypokalemia
low-renin hypertension
renal calcification
case series
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2024.1491825/full
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