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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.
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 ...
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]
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 ...
Central serous chorioretinopathy ( CSC or CSCR ), also known as central serous retinopathy ( CSR ), is an eye disease that causes visual impairment, often temporary, usually in one eye. [ 1][ 2] When the disorder is active it is characterized by leakage of fluid under the retina that has a propensity to accumulate under the central macula.
Congenital rubella syndrome. Congenital rubella syndrome (CRS) occurs when a human fetus is infected with the rubella virus (German measles) via maternal-fetal transmission and develops birth defects. [ 1] The most common congenital defects affect the ophthalmologic, cardiac, auditory, and neurologic systems. [ 2]
Saethre–Chotzen syndrome ( SCS ), also known as acrocephalosyndactyly type III, is a rare congenital disorder associated with craniosynostosis (premature closure of one or more of the sutures between the bones of the skull ). This affects the shape of the head and face, resulting in a cone-shaped head and an asymmetrical face.
The detached retina was caused by a cancerous tumor that had wrapped around Hensley’s optic nerve. She was diagnosed with ocular melanoma that began when the freckle in the back of her eye ...