Morvan syndrome: a rare cause of syndrome of inappropriate antidiuretic hormone secretion.

Clujul medical (1957) Pub Date : 2017-01-01 Epub Date: 2017-07-15 DOI:10.15386/cjmed-755
Seref Demirbas, Musa Baris Aykan, Haydar Zengin, Semir Mazman, Kenan Saglam
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引用次数: 2

Abstract

The syndrome of inappropriate antidiuretic hormone secretion (SIADH) accounts for an important part of hyponatremia cases. The causes of SIADH can be detected almost always. As a rare disorder, Morvan Syndrome can be defined by the sum of peripheral nerve hyperexcitability, autonomic instability and neuropsychiatric features. Antibodies to voltage-gated potassium channels (Anti - VGKC-Ab) including contactin associated protein-like 2 antibodies (CASPR2-Ab) and leucine-rich glioma inactivated protein 1 antibodies (LGI1-Ab) were previously known for the potential association with this condition. We present a Morvan Syndrome in a patient who presented with various neuropsychiatric symptoms and SIADH.

Morvan综合征:一种罕见的因抗利尿激素分泌不当引起的综合征。
抗利尿激素分泌不当综合征(SIADH)是低钠血症的重要组成部分。SIADH的病因几乎总是可以检测到的。作为一种罕见的疾病,Morvan综合征可以被定义为周围神经亢奋,自主神经不稳定和神经精神特征的总和。电压门控钾通道抗体(Anti - VGKC-Ab),包括接触蛋白相关蛋白样2抗体(CASPR2-Ab)和富含亮氨酸的胶质瘤失活蛋白1抗体(LGI1-Ab),此前已知与这种疾病有潜在关联。我们提出Morvan综合征患者谁提出了各种神经精神症状和SIADH。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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