Morvan Syndrome: A rare cause of syndrome of inappropriate antidiuretic hormone secretion
Clujul Medical, cilt.90, sa.3, ss.353-355, 2017 (Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 90 Sayı: 3
- Basım Tarihi: 2017
- Doi Numarası: 10.15386/cjmed-755
- Dergi Adı: Clujul Medical
- Derginin Tarandığı İndeksler: Scopus
- Sayfa Sayıları: ss.353-355
- Anahtar Kelimeler: Anti - VGKC-Ab, CASPR2-Ab, Hyponatremia, LGI1-Ab, Morvan Syndrome, SIADH
- Sağlık Bilimleri Üniversitesi Adresli: Evet
Özet
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.