Publication: Opsoclonus Myoclonus Ataxia Syndrome
| creativeworkseries.issn | ISSN 1990-7974 eISSN 1990-7982 | |
| dc.contributor.author | Kunchapudi, SK | |
| dc.contributor.author | Kumar, P | |
| dc.contributor.author | Sabharwal, RK | |
| dc.date.accessioned | 2026-03-23T07:18:10Z | |
| dc.date.available | 2026-03-23T07:18:10Z | |
| dc.date.issued | 2015 | |
| dc.description | SK Kunchapudi Department of Paediatric Neurology, Sir Ganga Ram Hospital, New Delhi P Kumar Consultant Neurologist, Department of Paediatric Neurology, Sir Ganga Ram Hospital, New Delhi RK Sabharwal Senior Consultant and Head, Department of Paediatric Neurology, Sir Ganga Ram Hospital, New Delhi | |
| dc.description.abstract | Abstract: Opsoclonus myoclonus ataxia syndrome (OMAS) is a rare neurological disorder predominantly affecting young children and causing severe neurological disability. Its early identification and treatment is advocated. Here we report a two year old child presenting with abnormal movements and subsequently developed features of OMAS and responding favourably to Adrenocorticotropic hormone (ACTH). | |
| dc.identifier | https://doi.org/10.3126/jnps.v35i1.11201 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14572/5350 | |
| dc.language.iso | en_US | |
| dc.publisher | Nepal Paediatric Society (JNPS) | |
| dc.subject | ACTH | |
| dc.subject | Neuroblastoma | |
| dc.subject | OMAS | |
| dc.subject | Opsoclonus | |
| dc.title | Opsoclonus Myoclonus Ataxia Syndrome | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.article.type | Case Report | |
| oaire.citation.endPage | 72 | |
| oaire.citation.startPage | 70 | |
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