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Updated: Sep 4, 2025

Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4
Published on: August 21, 2017
Familial Neuromyelitis Optica and Sjogren's Overlap Syndrome-A Rare Case Report
V H Ganaraja1, R Subasree1, M Netravathi1
1Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, Karnataka, India.
Familial Neuromyelitis Optica (NMO) with Sjogren's syndrome is rare. This study details a mother and daughter with NMO-Sjogren's overlap, highlighting potential shared genetic factors.
Area of Science:
- Neurology
- Immunology
- Genetics
Background:
- Neuromyelitis Optica (NMO) is a rare autoimmune disorder affecting the central nervous system.
- NMO is often associated with Aquaporin-4 (AQP4) antibodies.
- Co-occurrence of NMO and Sjogren's syndrome is infrequently reported, especially in familial cases.
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