Oculomotor Apraxia - American Association for Pediatric
what is oculomotor apraxia? Ocular motor apraxia (OMA) is a neurological disorder that causes problems with voluntary horizontal eye movement. Children with this condition have difficulty moving their eyes in a desired direction.
Oculomotor Apraxia - EyeWiki
Oculomotor apraxia (OMA) was first described in 1953 by American Ophthalmologist David Glendenning Cogan as a defect in, or absence of, the ability to perform voluntary eye movements. Affected patients are unable to willingly draw their eyes to an object that grabs their attention but can otherwise freely gaze left and right.
Oculomotor apraxia - Wikipedia
Oculomotor apraxia (OMA) is the absence or defect of controlled, voluntary, and purposeful eye movement. [1] It was first described in 1952 by the American ophthalmologist David Glendenning Cogan. [2] People with this condition have difficulty moving their …
What is Ocular Motor Apraxia? - News-Medical.net
2023年3月11日 · Ocular motor apraxia (OMA) is a neurological condition resulting in an inability to turn the eyes voluntarily in a horizontal manner. Ocular Motor Apraxia is known by a variety of terms....
Oculomotor apraxia: symptoms, treatment, and possible causes
2021年8月12日 · What is oculomotor apraxia and how does it affect eye movement? Let's look at the symptoms, treatments and possible causes of this disorder.
Eye Movement Disorders in Movement Disorders - PMC - PubMed …
Oculomotor apraxia can be identified during spontaneous gaze shifts if the head moves first and the eyes follow. Observe spontaneous gaze shift during history taking. Convergence (functional) spasm is associated with miosis in contrast to CN VI lesion.
Ocular motor apraxia, cogan type | About the Disease | GARD
Ocular motor apraxia, Cogan type is characterised by impairment of voluntary horizontal eye movements and compensatory head thrust. Around 50 cases have been described so far.
Oculomotor Apraxia - Eyes 4 Kids
2019年8月14日 · What is oculomotor apraxia? Ocular motor apraxia (OMA) is the absence of, or a defect in, the control of voluntary purposeful eye movement. Children with this condition have difficulty moving their eyes in a desired direction.
Oculomotor apraxia (Concept Id: C3489733) - National Center for ...
Ataxia-oculomotor apraxia-4 (AOA4) is an autosomal recessive neurologic disorder characterized by onset of dystonia and ataxia in the first decade. Additional features include oculomotor apraxia and peripheral neuropathy. Some patients may show cognitive impairment.
Oculomotor Apraxia | Hereditary Ocular Diseases
The genetics of isolated oculomotor apraxia is unknown since no responsible mutation has been identified. However, familial cases are known, including twins and sibling offspring of consanguineous matings, as well as multigenerational cases.