Opsoclonus Myoclonus Syndrome (OMS) is a rare neurological condition that affects the body’s movements and coordination. Kids with OMS may experience sudden jerky movements (myoclonus) and uncontrollable eye movements (opsoclonus).
Opsoclonus Myoclonus Syndrome (OMS) is a rare neurological condition that affects the body’s movements and coordination. Kids with OMS may experience sudden jerky movements (myoclonus) and uncontrollable eye movements (opsoclonus).
How is Opsoclonus Myoclonus Syndrome diagnosed?
Diagnosis involves a comprehensive evaluation by a healthcare professional experienced in neurodevelopmental disorders, which may include medical history, physical examination, neurological tests, and imaging studies.
Is Opsoclonus Myoclonus Syndrome a lifelong condition?
The long-term prognosis for OMS varies, but with early and comprehensive intervention, many children can experience significant improvement in symptoms and overall functioning. Regular follow-ups and continued therapies can contribute to positive outcomes.
Is Opsoclonus Myoclonus Syndrome hereditary?
OMS is not typically considered a hereditary condition. It usually occurs sporadically, without a family history. However, in rare cases, there may be a genetic predisposition or a link to specific genetic mutations.
Can Opsoclonus Myoclonus Syndrome affect adults as well?
While OMS is more commonly diagnosed in children, it can also affect adults, though it is rare. The symptoms and treatment approach may differ compared to cases in children.
Opsoclonus Myoclonus Syndrome (OMS) is a neurological disorder characterized by a combination of involuntary, rapid eye movements (opsoclonus) and sudden, jerky muscle movements (myoclonus). OMS is a rare condition whose exact cause is not fully understood. In most cases, it occurs in children, often under the age of 5 years, but it can also affect adults. Besides the motor symptoms, individuals with OMS may experience other neurological and behavioral issues. Early diagnosis and treatment by healthcare professionals specialized in neurodevelopmental disorders are crucial to managing OMS effectively.
Opsoclonus Myoclonus Syndrome (OMS) presents a range of symptoms that can be challenging to identify, especially for parents of kids with special needs. Here are some symptoms to watch out for:
Recognizing these symptoms early on can help parents seek medical attention promptly and start appropriate interventions to improve their child’s quality of life and overall well-being. Goally, a tablet with fun apps, helps kids with Opsoclonus Myoclonus Syndrome build life & language skills. Its features include visual schedules, AAC, emotional regulation, executive functioning, and social skills training videos.