<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Merati M</submitter><funding>NINDS NIH HHS</funding><pagination>278-281</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9620397</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>42(2)</volume><pubmed_abstract>&lt;h4>Abstract&lt;/h4>A 62-year-old man presented with headache, fever, and malaise. He was diagnosed with Anaplasma phagocytophilum, confirmed by serum polymerase chain reaction, and started on oral doxycycline. After 5 days of treatment, the patient began to experience gait imbalance with frequent falls, as well as myoclonus, and confusion. Examination was notable for opsoclonus-myoclonus-ataxia (OMA) and hypometric saccades. Cerebrospinal fluid (CSF) autoimmune encephalitis panel demonstrated a markedly elevated neuronal intermediate filament (NIF) immunoglobulin G antibody titer of 1:16, with positive neurofilament light- and heavy-chain antibodies. These antibodies were suspected to have been triggered by the Anaplasma infection. Repeat CSF examination 8 days later still showed a positive </pubmed_abstract><journal>Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society</journal><pubmed_title>A Case of Opsoclonus-Myoclonus-Ataxia With Neuronal Intermediate Filament IgG Detected in Cerebrospinal Fluid.</pubmed_title><pmcid>PMC9620397</pmcid><funding_grant_id>R01 NS126227</funding_grant_id><pubmed_authors>Balcer LJ</pubmed_authors><pubmed_authors>McKeon A</pubmed_authors><pubmed_authors>Frucht SJ</pubmed_authors><pubmed_authors>Hu J</pubmed_authors><pubmed_authors>Rucker JC</pubmed_authors><pubmed_authors>Galetta SL</pubmed_authors><pubmed_authors>Merati M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Case of Opsoclonus-Myoclonus-Ataxia With Neuronal Intermediate Filament IgG Detected in Cerebrospinal Fluid.</name><description>&lt;h4>Abstract&lt;/h4>A 62-year-old man presented with headache, fever, and malaise. He was diagnosed with Anaplasma phagocytophilum, confirmed by serum polymerase chain reaction, and started on oral doxycycline. After 5 days of treatment, the patient began to experience gait imbalance with frequent falls, as well as myoclonus, and confusion. Examination was notable for opsoclonus-myoclonus-ataxia (OMA) and hypometric saccades. Cerebrospinal fluid (CSF) autoimmune encephalitis panel demonstrated a markedly elevated neuronal intermediate filament (NIF) immunoglobulin G antibody titer of 1:16, with positive neurofilament light- and heavy-chain antibodies. These antibodies were suspected to have been triggered by the Anaplasma infection. Repeat CSF examination 8 days later still showed a positive </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2025-04-27T02:14:54.447Z</modification><creation>2025-04-06T18:33:19.941Z</creation></dates><accession>S-EPMC9620397</accession><cross_references><pubmed>35594157</pubmed><doi>10.1097/wno.0000000000001599</doi><doi>10.1097/WNO.0000000000001599</doi></cross_references></HashMap>