AN EARLY FAMILY HISTORY OF COLOR BLINDNESS
نویسندگان
چکیده
منابع مشابه
Color-Vision and Color-Blindness
Special public attention was called to the subject in 1875 by an enquiry into the causes of a railway accident which had taken place in Sweden, from which it appears that colourblindness was the cause of the disaster. Our author having described colour-sensations, goes on to discuss the theories of colour-perception and colour-blindness, classifying the latter defect as total and partial. Total...
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Achromatopsia is a rare congenital cause of vision loss due to isolated cone photoreceptor dysfunction. The most common underlying genetic mutations are autosomal recessive changes in CNGA3, CNGB3, GNAT2, PDE6H, PDE6C, or ATF6. Animal models of Cnga3, Cngb3, and Gnat2 have been rescued using AAV gene therapy; showing partial restoration of cone electrophysiology and integration of this new phot...
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Background and aims: Color blindness is a disease that remains undiagnosed in some cases. Thediagnosis of the disease during schooling is necessary to take the required measures for the future lifeof adolescents. Therefore, the aim of this study was to determine the prevalence of color blindnessamong the students of secondary schools in Shahrekord.Methods: In this descri...
متن کاملColor blindness and its illuminations
In 1974, not long after an antenna was implanted in his skull, the British artist Neil Harbisson became the first person in history to be officially recognized as a cyborg.1 A cyborg—short for cybernetic organism—is a living thing formed from the integration of organic and mechanical parts. Before becoming a cyborg, Harbisson struggled as an art student afflicted with achromatopsia, an extremel...
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ژورنال
عنوان ژورنال: Journal of Heredity
سال: 1919
ISSN: 1465-7333,0022-1503
DOI: 10.1093/oxfordjournals.jhered.a101950