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Infant visual development. A seven-week-old human baby following a kinetic object. Infant vision concerns the development of visual ability in human infants from birth through the first years of life. The aspects of human vision which develop following birth include visual acuity, tracking, color perception, depth perception, and object ...
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.
Childhood blindness is an important contribution to the national prevalence of the disability of blindness. [ 3] Blindness in children can be defined as a visual acuity of <3/60 in the eye with better vision of a child under 16 years of age. [ 4] This generally means that the child cannot see an object 10 feet (about 3 meters) away, that ...
Specialty. Ophthalmology. Retinopathy of prematurity ( ROP ), also called retrolental fibroplasia ( RLF) and Terry syndrome, is a disease of the eye affecting prematurely born babies generally having received neonatal intensive care, in which oxygen therapy is used because of the premature development of their lungs. [ 2]
Neonatal jaundice is a yellowish discoloration of the white part of the eyes and skin in a newborn baby due to high bilirubin levels. [ 1] Other symptoms may include excess sleepiness or poor feeding. [ 1] Complications may include seizures, cerebral palsy, or kernicterus. [ 1]
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 ...
CHARGE syndrome (formerly known as CHARGE association) is a rare syndrome caused by a genetic disorder.First described in 1979, the acronym "CHARGE" came into use for newborn children with the congenital features of coloboma of the eye, heart defects, atresia of the nasal choanae, restricted growth or development, genital or urinary abnormalities, and ear abnormalities and deafness. [1]
Global developmental delay is an umbrella term used when children are significantly delayed in two or more areas of development. It can be diagnosed when a child is delayed in one or more milestones, categorised into motor skills, speech, cognitive skills, and social and emotional development. [ 1] There is usually a specific condition which ...