[Opsoclonus-myoclonus syndrome in children]
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova
|April 2, 2008
Summary
Parainfectious opsoclonus-myoclonus syndrome (OMS) in children often follows viral infections or vaccinations, presenting unique clinical features. Early treatment with hormonal therapy and immunomodulators shows promise for managing this rare neurological disorder.
Area of Science:
- Pediatric Neurology
- Neuroimmunology
- Infectious Diseases
Background:
- Parainfectious opsoclonus-myoclonus syndrome (OMS) is a rare autoimmune neurological disorder typically affecting young children.
- The etiology is often linked to preceding viral infections or vaccinations, triggering an immune response against the nervous system.
Purpose of the Study:
- To investigate the clinical characteristics of parainfectious OMS in children.
- To explore effective pharmacotherapeutic strategies for managing OMS in pediatric patients.
Main Methods:
- Neurological, neurophysiological, immunological, and virological examinations were performed on 20 children diagnosed with OMS.
- Magnetic resonance tomography (MRT) was utilized to assess for specific brain changes.
- Age at onset ranged from 8 months to 3 years, with a noted seasonality (autumn, spring).
Main Results:
- A significant proportion of cases (55%) were associated with prior viral infections, and 15% with vaccination.
- Virological and immunological studies supported the role of infectious factors in disease development.
- Brain MRT revealed an absence of specific changes, and cerebrospinal fluid abnormalities were infrequent.
Conclusions:
- Parainfectious OMS in children exhibits distinct clinical features and is often triggered by infections or vaccinations.
- The study highlights positive outcomes using hormonal therapy and immunomodulators for pharmacotherapeutic correction.
- Further research into the immunopathogenesis and treatment of OMS is warranted.
More Related Videos
Related Concept Videos
Seizures: Classification
Epilepsy is primarily characterized by unpredictable seizures, either provoked by an identifiable factor, such as injury or illness, or unprovoked, occurring spontaneously without apparent cause.
Seizures are typically classified into two main categories: focal and generalized seizures.
Focal Seizures
Focal seizures originate from specific regions of the brain. These seizures are further sub-classified into two types:
Seizures are typically classified into two main categories: focal and generalized seizures.
Focal Seizures
Focal seizures originate from specific regions of the brain. These seizures are further sub-classified into two types:
Sleep-Wake Cycles
Sleep is an essential physiological process vital to maintaining overall well-being. The reticular activating system (RAS), a network of neurons in the brainstem, regulates wakefulness and sleep. While it may seem passive, sleep consists of distinct cycles, each with its unique characteristics and functions. Two key sleep phases are non-rapid eye movement (NREM) and rapid eye movement (REM).
NREM Sleep
NREM sleep comprises four progressive stages that seamlessly merge:
NREM Sleep
NREM sleep comprises four progressive stages that seamlessly merge:
Seizures ll: Types
Seizures are sudden bursts of abnormal electrical discharge in the brain that interfere with normal function. They are commonly divided into three groups: focal seizures, generalized seizures, and other types that do not fit neatly into either category.Focal SeizuresFocal seizures begin in a single brain region. When awareness is preserved, they are called focal aware seizures and may cause sensations such as tingling, unusual smells, or flashing lights. When awareness is impaired, they are...
Epilepsy and Seizures: Overview
Epilepsy is a chronic neurological disease marked by recurrent, unpredictable seizures. These seizures are caused by abnormal electrical discharges in the brain, leading to behavior, sensation, or consciousness alterations. They can also cause transient impairment of awareness, interfering with daily activities.
Various factors can trigger epilepsy, including genetic factors, brain damage, metabolic causes, and unknown etiology. Diagnosis of epilepsy involves electroencephalography (EEG), which...
Various factors can trigger epilepsy, including genetic factors, brain damage, metabolic causes, and unknown etiology. Diagnosis of epilepsy involves electroencephalography (EEG), which...
Oppositional Defiant Disorder
A persistent pattern of angry or irritable mood, defiant behavior, or vindictiveness characterizes Oppositional Defiant Disorder (ODD). Symptoms must occur over at least six months, involve interactions with individuals beyond siblings, and meet specific diagnostic criteria to be clinically significant. The disorder affects emotional regulation, social interactions, and behavior, often manifesting early in life and influencing long-term development and functioning.
Diagnostic Criteria and...
Diagnostic Criteria and...
Restless Leg Syndrome and Night Terrors
Restless Leg Syndrome (RLS), also known as Willis-Ekbom disease, is a neurological disorder characterized by an uncontrollable urge to move the legs due to uncomfortable sensations. These sensations typically occur during periods of rest or inactivity, particularly when lying down or sitting, and can severely disrupt sleep.
The exact cause of RLS is not fully understood, but it is believed to involve dopamine, a neurotransmitter that helps regulate muscle movement. Imbalances in dopamine levels...
The exact cause of RLS is not fully understood, but it is believed to involve dopamine, a neurotransmitter that helps regulate muscle movement. Imbalances in dopamine levels...


