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Amblyopia, also called lazy eye, is a disorder of sight in which the brain fails to fully process input from one eye and over time favors the other eye. [ 1] It results in decreased vision in an eye that typically appears normal in other aspects. [ 1] Amblyopia is the most common cause of decreased vision in a single eye among children and ...
Frequency. ~2% (children) [ 3] Strabismus is a vision disorder in which the eyes do not properly align with each other when looking at an object. [ 2] The eye that is pointed at an object can alternate. [ 3] The condition may be present occasionally or constantly. [ 3] If present during a large part of childhood, it may result in amblyopia, or ...
The management of strabismus may include the use of drugs or surgery to correct the strabismus. Agents used include paralytic agents such as botox used on extraocular muscles, [1] topical autonomic nervous system agents to alter the refractive index in the eyes, and agents that act in the central nervous system to correct amblyopia. [2]
Childhood cataracts are the primary cause of childhood blindness. [4] Childhood cataracts make up 7.4% to 15.3% of blindness in kids. [4] The prevalence of childhood cataracts ranges from 0.63/10,000 to 9.74/10,000 children, with a median of 1.71. [6] This is dependent on factors like economic status but not gender or laterality. [6]
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FM channel 200, 87.9 MHz, overlaps TV 6. This is used only by K200AA.Channel 6A is only used in South Korea, and the Philippines. TV 6 analog audio can be heard on FM 87.75 on most broadcast radio receivers as well as on a European TV tuned to channel 4A or channel C, but at lower volume than wideband FM broadcast stations, because of the lower deviation.
Strabismus can occur due to problems with the muscles and nerves that control the eyes, as a side effect of an eye injury or other medical condition, or as a complication from significant far ...
Down syndrome (United States) or Down's syndrome (United Kingdom and other English-speaking nations), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. [ 3] It is usually associated with developmental delays, mild to moderate intellectual disability, and characteristic ...