What is the prevalence of Ocular Motor Apraxia?
How many people does Ocular Motor Apraxia affect? Does it have the same prevalence in men and women? And in the different countries?
Ocular Motor Apraxia (OMA) is a rare neurological disorder that affects voluntary eye movements. It is characterized by the inability to accurately move the eyes horizontally or vertically, leading to difficulty in tracking objects or shifting gaze. The prevalence of OMA is not well-established due to its rarity and underdiagnosis. However, studies suggest that it affects a small percentage of the population, estimated to be less than 1%. OMA is often associated with other neurological conditions, such as ataxia or developmental disorders. Early diagnosis and appropriate management can help individuals with OMA improve their eye coordination and quality of life.
Ocular Motor Apraxia (OMA) is a rare neurological disorder that affects eye movements. It is characterized by the inability to voluntarily move the eyes in a coordinated manner, despite normal eye function and vision. OMA is typically present from birth or early childhood and can be caused by genetic mutations or acquired brain injuries.
The prevalence of OMA is not well-established due to its rarity and underdiagnosis. However, studies suggest that it affects approximately 1 in 10,000 to 1 in 100,000 individuals. The condition may be more prevalent in certain populations or specific genetic disorders, such as ataxia-telangiectasia.
OMA can significantly impact daily activities that require precise eye movements, such as reading, driving, or playing sports. Individuals with OMA may experience difficulties with visual tracking, coordination, and depth perception. Early diagnosis and intervention, including occupational therapy and visual aids, can help manage the symptoms and improve quality of life.
While OMA is a rare condition, it is important to raise awareness and support research efforts to better understand its prevalence, causes, and potential treatments.
