Publication:
Opsoclonus Myoclonus Ataxia Syndrome

Date

2015

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Publisher

Nepal Paediatric Society (JNPS)

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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).

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

Keywords

ACTH, Neuroblastoma, OMAS, Opsoclonus

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