This is because other unexpected manifestations can also occur, such as area postrema syndrome APS , the imaging characteristics of chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids CLIPPERS , meningoencephalitis, ADEM-like form presentations, leukodystrophy, and peripheral nervous system involvement —.
However, in the absence of large-size, multi-center studies, the current study expanded the clinical features and added data to long-term outcomes of MOGAD.
Serum anti-streptolysin O was found in 1 patient, and another patient tested seropositive for anti-Smith antibody.
MOG-IgG should be tested in patients presenting with APS because MOGAD differs from NMOSD in terms of treatment and prognosis.
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A total of 19 70% patients were women, the median age at disease onset was 40 years range 20—67.