Opsoclonus-Myoclonus-Ataxia Syndrome (OMAS) - Children's …
Opsoclonus-myoclonus-ataxia syndrome (often referred to as OMAS or opsoclonus-myoclonus syndrome) is an autoimmune disorder of the nervous system characterized by new movements of the limbs and eyes, abnormal behaviors, sleep dysregulation, and difficulty talking.
Opsoclonus myoclonus syndrome - Wikipedia
Opsoclonus myoclonus syndrome (OMS), also known as opsoclonus-myoclonus-ataxia (OMA), is a rare neurological disorder of unknown cause which appears to be the result of an autoimmune process involving the nervous system. It is an extremely rare condition, affecting as few as 1 in 10,000,000 people per year.
Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia …
Opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare disorder of the nervous system that classically presents with a combination of characteristic eye movement disorder and myoclonus, in addition to ataxia, irritability, and sleep disturbance.
Opsoclonus-myoclonus-ataxia syndrome - UpToDate
2024年10月7日 · Opsoclonus-myoclonus-ataxia syndrome (OMAS), also known as opsoclonus-myoclonus, is a rare and debilitating acquired nervous system disorder characterized by opsoclonus, diffuse or focal body myoclonus, and truncal titubation with or without ataxia and other cerebellar signs.
Opsoclonus-Myoclonus-Ataxia Syndrome - Symptoms, Causes, …
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Diagnosis and Management of Opsoclonus-Myoclonus-Ataxia …
2022年3月8日 · Background and objectives: Opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare disorder of the nervous system that classically presents with a combination of characteristic eye movement disorder and myoclonus, in addition to ataxia, irritability, and sleep disturbance.
Opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare disorder of the nervous system that classically presents with a combination of characteristic eye movement disorder and myoclonus, in addition to ataxia, irritability, and sleep disturbance.
Opsoclonus–myoclonus–ataxia syndrome in children
2021年3月29日 · Opsoclonus–myoclonus–ataxia syndrome is a rare neuroimmunologic disorder typically presenting in previously healthy infants and toddlers. It is characterized by a clinical triad of (1) erratic saccadic intrusions; (2) myoclonus and/or ataxia; (3) behavioral features, typified by developmental plateauing, irritability and insomnia.
Adult-onset opsoclonus-myoclonus-ataxia syndrome as a …
2014年3月31日 · OMAS is a rare and debilitating neurologic disease, showing acute or subacute onset in childhood or adult life, occurring in 1–2 people per 10 million per year. 9-11 Opsoclonus is an important marker and a diagnostic clue for this syndrome.
A Rare Case of Opsoclonus Myoclonus Ataxia Syndrome Post Viral …
Opsoclonus myoclonus ataxia syndrome (OMAS) is a rare inflammatory neurological disorder characterized by ocular, motor, behavioral, language, and sleep disturbances. It usually affects infants and young children but may affect adults.