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. 2017 Feb 16;8:25. doi: 10.3389/fpsyt.2017.00025

Table 3.

Clinical symptoms and constellations that led to the determination of anti-neuronal antibodies in all 100 patients.

Symptoms All patients (100) NMDAR (53) Non-NMDAR (24) Intracellular antigens (23)
Epileptic seizures 14 (14%) 10 (19%) 2 (8%) 2 (8%)
Cerebrospinal fluid (CSF) abnormalitiesa and absent evidence for infectious encephalitis 13 (13%) 12 (27%) 1 (4%)
Abnormal postures or movements 4 (4%) 4 (7%)
Reduced levels of consciousness 4 (4%) 4 (7%)
Aphasia or dysarthria 3 (3%) 3 (6%)
Lack of improvement with antipsychotics 5 (5%) 4 (7%) 1 (4%)
Autonomic instability 2 (2%) 2 (4%)
Suspicious MRI or EEG findings 10 (10%) 3 (6%) 5 (20%) 2 (8%)
Steroid-responsive autoimmune thyroiditis 3 (3%) 2 (4%) 1 (4%)
Lack of improvement with antiepileptic medication 2 (2%) 1 (2%) 1 (4%)
Focal neurological deficits 3 (3%) 1 (2%) 1 (4%) 1 (4%)
Sensory deficits 3 (3%) 1 (2%) 2 (8%)
Rapidly progressing psychosis 4 (4%) 1 (2%) 2 (8%) 1 (4%)
Suggested by patients or families 3 (3%) 3 (6%)
Positive effect of ex juvantibus immunotherapy 2 (2%) 1 (4%) 1 (4%)
Faciobrachial dystonic seizures 3 (3%) 3 (12%)
Neuromyotonia 1 (1%) 1 (4%)
Cerebellar ataxia 8 (8%) 2 (8%) 6 (26%)
Hyponatremia 2 (2%) 2 (8%)
Paresthesia or malignant tumorb 7 (7%) 7 (30%)

aIncreased white blood cell count or CSF-specific oligoclonal bands.

bSmall-cell lung cancer, testicular seminoma.