| CASE REPORT |
|
| Year : 2022 | Volume
: 5
| Issue : 2 | Page : 121-124 |
|
|
Faciobrachial dystonic seizure-like events in a patient with subacute sclerosing panencephalitis
Vikram V Holla1, Sudhakar Pushpa Chaithra1, Shweta Prasad2, Nitish Kamble1, Pramod Kumar Pal1, Ravi Yadav1
1 Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, Karnataka, India
2 Clinical Neurosciences and Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, Karnataka, India
Correspondence Address:
Dr. Ravi Yadav
Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru - 560029, Karnataka
India
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/AOMD.AOMD_41_21
|
|
|
Faciobrachial dystonic seizure is a distinctive phenomenology that is considered pathognomonic of leucine-rich glioma-inactivated protein 1 (LGI1) antibody-associated autoimmune limbic encephalitis. However, similar phenomenology has been described with other neurological disorders as well. Here, we report the case of a 26-year-old man with subacute sclerosing panencephalitis who presented with multiple episodes of involuntary movements resembling faciobrachial dystonic seizure. Serum and cerebrospinal fluid autoimmune encephalitis panel, including leucine-rich glioma-inactivated protein 1 antibody, were negative. Classical periodic stereotypical slow wave discharges on the electroencephalogram and raised measles antibody titre in cerebrospinal fluid confirmed the diagnosis of subacute sclerosing panencephalitis. |
|
|
|
| [FULL TEXT] [PDF]* |
|
 |
|
