Annals of Movement Disorders (Jan 2022)

Hyperammonemia presenting as opsoclonus–myoclonus–ataxia–tremor syndrome: A case report

  • Sandhya Manorenj,
  • Govind Verma

DOI
https://doi.org/10.4103/aomd.aomd_6_22
Journal volume & issue
Vol. 5, no. 3
pp. 198 – 201

Abstract

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Opsoclonus myoclonus syndrome (OMS) is a rare autoimmune condition occurring due to Purkinje cell degeneration due to remote aetiology. Most often it occurs as a paraneoplastic syndrome. Here we report a case of opsoclonus-myoclonus–ataxia tremor syndrome in a 60-year-old woman that occurred due to hyperammonemia and she recovered completely with immunotherapy and correction of hyperammonemia. OMS is the first in literature associated with hyperammonemia.

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