假性醛固酮减少症I型的部分形式,无肾钠消耗。

A Ballauff, U Wendel, I Kupke, U Kuhnle
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引用次数: 3

摘要

假性醛固酮减少症涉及多个目标器官是已知的,但部分缺陷只涉及单一器官系统也被描述过。在这个报告中,我们提出了一个女孩的早期症状和一个非常轻微的病程,没有肾盐消耗和正常的汗液渗透压。大便钠含量和钠钾比明显升高。血浆肾素活性和醛固酮浓度升高以及单核白细胞醛固酮受体数量减少证实了假性醛固酮减少症的诊断。部分假性醛固酮减少症可能比目前诊断的更频繁,因为盐的损失可以通过完整的器官系统来补偿,但在疾病期间仍然威胁着年轻患者。由于假性醛固酮增多症的临床严重程度不同,即使在同一个家庭也有记载,因此为了监测年幼的兄弟姐妹,确定轻度病例似乎很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A partial form of pseudohypoaldosteronism type I without renal sodium wasting.

Multiple target organ involvement in pseudohypoaldosteronism is known but partial defects involving only a single organ system have also been described. In this report we present a girl with early symptoms and a very mild course of the disease without renal salt wasting and with normal sweat osmolality. Sodium content and the sodium/potassium ratio of stool was highly elevated. Increased plasma renin activity and aldosterone concentration as well as a reduced number of aldosterone receptors in mononuclear leucocytes confirmed the diagnosis of pseudohypoaldosteronism. Partial pseudohypoaldosteronism maybe more frequent than currently diagnosed since salt loss can be compensated by intact organ systems, but nevertheless threatens the young patient during illness. Since various degrees of clinical severity of pseudohypoaldosteronism even in the same family have been described, it seems important to identify mild cases in order to monitor younger siblings.

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