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Diagnosis of convergence insufficiency is made by an eye care professional skilled in binocular vision dysfunctions, such as an optometrist, ophthalmologist, or orthoptist to rule out any organic disease. Convergence insufficiency is characterized by one or more of the following diagnostic findings: patient symptoms, high exophoria at near ...
Anisometropia causes some people to have mild vision problems, or occasionally more serious symptoms like alternating vision or frequent squinting. However, since most people do not show any clear symptoms, the condition usually is found during a routine eye exam. [8] For early detection in preverbal children, photoscreening can be used.
In ophthalmology, Functional visual loss is the reduction in visual acuity or visual field that has no physiological or organic basis. This disease can come under the spectrum of functional neurological disorder or somatic symptom disorder under the categorization of the Diagnostic and Statistical Manual of Mental Disorders -5.
Visual impairment. Visual or vision impairment ( VI or VIP) is the partial or total inability of visual perception. In the absence of treatment such as corrective eyewear, assistive devices, and medical treatment, visual impairment may cause the individual difficulties with normal daily tasks, including reading and walking. [ 6]
Genetic disorders often cause eye problems for affected children. Since approximately 30% of genetic syndromes affect the eyes, examination by a pediatric ophthalmologist can help with the diagnosis of genetic conditions. Many pediatric ophthalmologists participate with multi-disciplinary medical teams that treat children with genetic syndromes.
Secondary glaucoma is a progressive optic nerve disorder which results in complete loss of vision. Secondary glaucoma is a collection of progressive optic nerve disorders associated with a rise in intraocular pressure (IOP) which results in the loss of vision. In clinical settings, it is defined as the occurrence of IOP above 21 mmHg requiring ...
When refractive errors in children are not treated, the child may be at risk of developing ambylopia, where vision may remain permanently blurry. [19] Because young children typically do not complain of blurry vision, the American Academy of Pediatrics recommends that children have yearly vision screening starting at three years old so that unknown refractive errors or other ophthalmic ...
Congenital blindness is a hereditary disease and can be treated by gene therapy. Visual loss in children or infants can occur either at the prenatal stage (during the time of conception or intrauterine period) or postnatal stage (immediately after birth). [3] There are multiple possible causes of congenital blindness.