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Several blind characters have been created by Marvel Comics, including Daredevil, Blind Al, Blindfold, Destiny, Madame Web, and Julia Carpenter. Blind characters created by DC Comics include Doctor Mid-Nite and Crazy Quilt. Kenshi Takahashi is a blind swordsman created for the Mortal Kombat video game series.
People's poor ability to detect changes has been argued to reflect fundamental limitations of human attention. Change blindness has become a highly researched topic and some have argued that it may have important practical implications in areas such as eyewitness testimony and distractions while driving.
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]
Dichromacy in humans is a form of color blindness (color vision deficiency). Normal human color vision is trichromatic, so dichromacy is achieved by losing functionality of one of the three cone cells. The classification of human dichromacy depends on which cone is missing:
Kallmann syndrome (KS) is a genetic disorder that prevents a person from starting or fully completing puberty.Kallmann syndrome is a form of a group of conditions termed hypogonadotropic hypogonadism. [1]
Visual impairment in art is a limited topic covered by research, with its focus being on how visually impaired people are represented in artwork throughout history. This is commonly portrayed through the inclusion of objects such as canes and dogs to symbolize blindness, [1] which is the most frequently depicted visual impairment in art.
Retinitis pigmentosa is the leading cause of inherited blindness, [51] with approximately 1/4,000 individuals experiencing the non-syndromic form of their disease within their lifetime. [52] It is estimated that 1.5 million people worldwide are currently affected.
Usher syndrome, also known as Hallgren syndrome, Usher–Hallgren syndrome, retinitis pigmentosa–dysacusis syndrome or dystrophia retinae dysacusis syndrome, [1] is a rare genetic disorder caused by a mutation in any one of at least 11 genes resulting in a combination of hearing loss and visual impairment.