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

Autor:	Sandhya Manorenj, Govind Verma
Jazyk:	angličtina
Rok vydání:	2022
Předmět:	ataxia hyperammonemia myoclonus opsoclonus Neurology. Diseases of the nervous system RC346-429
Zdroj:	Annals of Movement Disorders, Vol 5, Iss 3, Pp 198-201 (2022)
Druh dokumentu:	article
ISSN:	2590-3446 2590-3454
DOI:	10.4103/aomd.aomd_6_22
Popis:	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.
Databáze:	Directory of Open Access Journals
Externí odkaz:	https://doaj.org/article/efae317c1e8d4b5a984c4ed565ca153a Zobrazit plný text záznamu View record in DOAJ