MORVAN SYNDROME: A RARE CAUSE OF SYNDROME OF INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION

Authors

DOI:

https://doi.org/10.15386/cjmed-755

Keywords:

hyponatremia, SIADH, Morvan Syndrome, CASPR2-Ab, anti – VGKC-Ab, LGI1-Ab

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. 


Author Biographies

Seref Demirbas, GULHANE TRAINING AND RESEARCH HOSPITAL

DEPARTMENT OF INTERNAL MEDICINE

Musa Baris Aykan, GULHANE TRAINING AND RESEARCH HOSPITAL

DEPARTMENT OF INTERNAL MEDICINE

Haydar Zengin, GULHANE TRAINING AND RESEARCH HOSPITAL

DEPARTMENT OF INTERNAL MEDICINE

Semir Mazman, GULHANE TRAINING AND RESEARCH HOSPITAL

DEPARTMENT OF NEUROLOGY

Kenan Saglam, GULHANE TRAINING AND RESEARCH HOSPITAL

DEPARTMENT OF INTERNAL MEDICINE

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Published

2017-07-25

How to Cite

1.
Demirbas S, Aykan MB, Zengin H, Mazman S, Saglam K. MORVAN SYNDROME: A RARE CAUSE OF SYNDROME OF INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION. Med Pharm Rep [Internet]. 2017 Jul. 25 [cited 2025 Oct. 5];90(3):353-5. Available from: https://medpharmareports.com/index.php/mpr/article/view/755

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Section

Case Report