Downloads: 7
Informative Article | Medicine | Volume 13 Issue 6, June 2024 | Pages: 1814 - 1815 | India
Rare Case of Seronegative Neuromyelitis Optica Presenting with Seizure
Abstract: Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune condition primarily characterized by optic neuritis and longitudinally extensive transverse myelitis (LETM). Seropositivity for aquaporin-4 antibodies (AQP4-IgG) has been considered a hallmark of NMOSD. However, this case presentation focuses on an exceptional case of NMOSD in a 28 year old female presenting with 1st episode of seizure who didn?t exhibit evidence of AQP4-IgG seropositivity. Keywords ? Seronegative Neuromyelitis Optica ? Generalized Tonic-Clonic Seizures.
Keywords: Seronegative Neuromyelitis Optica, Generalized Tonic-Clonic Seizures, Atypical NMO Presentation, AQP4-IgG Negative, Autoimmune Neurological Disorder
How to Cite?: Dr. Raj Sachde, Dr Subhashchandra K Gadhvicharan, Dr. Girish Kalsariya, "Rare Case of Seronegative Neuromyelitis Optica Presenting with Seizure", Volume 13 Issue 6, June 2024, International Journal of Science and Research (IJSR), Pages: 1814-1815, https://www.ijsr.net/getabstract.php?paperid=MR24628132218, DOI: https://dx.doi.org/10.21275/MR24628132218