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. 2021 Nov 22;12:761354. doi: 10.3389/fimmu.2021.761354

Table 2.

Summary of clinical syndromes and associated conditions in patients with GFAP Astrocytopathy.

Feature Incidence Slow wave+epileptiform discharge 6/31 (19.35%)
Males: females 23:12 Neuroimaging
Mean age 6.3 ± 0.6 Brain 29/35 (82.86%)
Intensive care unit 11/35 (31.43%) Periventricular radial linear
enhancement
3/35 (8.57%)
Early symptoms (runny nose, sore throat, cough, etc.) 9/35 (25.71%) enhancement of other parts 12/35 (34.29%)
Clinical syndrome spinal cord 9/35 (25.71%)
Meningoencephalitis 20/35 (57.14%) optic nerve 7/35 (20%)
Meningeal encephalomyelitis 7/35 (20%) CSF
Myelitis 1/35 (2.86%) Normal leukocyte 12/35 (34.29%)
Main symptoms Elevated leukocyte 23/35 (65.71%)
Fever 22/35 (62.86%) Tumor 2/35 (5.71%)
Headache 15/35 (42.86%) Multiple antibodies positive 11/35 (31.43%)
Seizures 15/35 (42.86%) Therapy
psychosis 18/35 (51.43%) IVMP 7/35 (20%)
Disorder of consciousness 19/35 (54.29%) IVIG 3/35 (8.57%)
optic neuritis 8/35 ( (22.86%) IVMP+IVIG 21/35 (60%)
ataxia 4/35 (11.43%) IVMP, IVIG+Second-line immunomodulatory therapy 4/35 (11.43%)
dyskinesia 14/35 (40.00%) IVMP,IVIG+PLEX 1/35 (2.86%)
Autonomic nerve dysfunction 9/35 (25.71%) mRS
peripheral nerve damage 3/35 (8.57%) On admission mRS (0-3) 17/35 (48.57%)
EEG findings On admission mRS (4-5) 18/35 (51.43%)
Normal 5/31 (16.12%) At discharge mRS (0-2) 26/35 (74.29%)
Slow wave background 19/31 (61.29%) At discharge mRS (3-5) 9/35 (25.71%)