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Opsoclonus myoclonus syndrome

rare disease

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Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionJun 2, 2025
Entity authorityQ1424706 ↗
Source-derived summary

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. It affects 2 to 3% of children with neuroblastoma and has been reported to occur with celiac disease and diseases of neurologic and autonomic dysfunction.

Signs and symptoms

Symptoms include:

opsoclonus (rapid, involuntary, multivectorial (horizontal and vertical), unpredictable, conjugate fast eye movements without intersaccadic [quick rotation of the eyes] intervals)

myoclonus (brief, involuntary twitching of a muscle or a group of muscles)

cerebellar ataxia, both truncal and appendicular

aphasia (a language disorder in which there is an impairment of speech and of comprehension of speech, caused by brain damage)

mutism (a language disorder in which a person does not speak despite evidence of speech ability in the past, often part of a larger neurological or psychiatric disorder)

lethargy

irritability or malaise

drooling

strabismus (a condition in which the eyes are not properly aligned with each other)

vomiting

sleep disturbances

emotional disturbances (including fits of rage)

About half of all OMS cases occur in association with neuroblastoma (a cancer of the sympathetic nervous system usually occurring in infants and children).

Disease course and clinical subtypes

In most cases, OMS starts with an acute flare-up of physical symptoms within days or weeks, but some less obvious symptoms such as irritability and malaise may begin weeks or months earlier.

Cause

In children, most cases are associated with neuroblastoma and most of the others are suspected to be associated with a low-grade neuroblastoma that spontaneously regressed before detection. In adults, most cases are associated with breast carcinoma or small-cell lung carcinoma. It is one of the few paraneoplastic (meaning 'indirectly caused by cancer') syndromes that occurs in both children and adults, although the mechanism of immune dysfunction underlying the adult syndrome is probably quite different.

It is hypothesized that a viral infection (perhaps St. Louis encephalitis, Chikungunya, Epstein-Barr, Coxsackie B, enterovirus, or just a flu) causes the remaining cases, though a direct connection has not been proven.

Editorial summary

This brief starts where responsible research should: with the source description of “Opsoclonus myoclonus syndrome” as rare disease. Everything that follows is an evidence route, not borrowed authority.

Editorial reviewA concise reference frame for defining the subject, testing terminology and identifying the institution closest to the evidence. The current 360-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. The account is most persuasive where Opsoclonus, myoclonus and syndrome can be independently traced.
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Why this record matters

The subject matters to the general reference register because the source frames it as rare disease. Its deeper value depends on whether names, dates, institutions and citations support that framing.

Evidence profile

The citation trail is more important than the brevity of the summary: it shows where individual claims can be examined in context. The source revision retrieved here is dated Jun 2, 2025. The linked authority identifier is Q1424706. None of the 0 selected statements returned an explicit reference.

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Source & attribution

This entry incorporates text from “Opsoclonus myoclonus syndrome” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.