A Study on Prevalence of Colour Vision Defects and Correlation with Sex, Visual Acuity and Blood Groups of the Study Group

I. V. Padma, S. Panda
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引用次数: 1

Abstract

Inherited color blindness is a lifelong challenge. While it may limit prospects for certain jobs, most peoplefind ways to adapt to the condition. Colour vision defect is usually for red-green colour and it is X-linkedrecessive trait. It is mainly homozygous that develop colour vision defects. Female heterozygous usuallyhave normal vision. Colour vision defects also have a strong genetic component , especially if both parentshave colour vision defects , and people with a particular blood group , and very myopic or hypermetropic, there is a good chance their child will be same. Color blindness is often apparent at a young age whenchildren are learning their colours and goes undetected because as they grow they learn to associate specificcolours with certain objects.For example, they come to know that grass is green, so they call the colour theysee green. If symptoms are very mild, a person may not realize that they don’t see certain colours.
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色觉缺陷患病率及其与性别、视力、血型的相关性研究
遗传性色盲是一项终身挑战。虽然这可能会限制某些工作的前景,但大多数人都会找到适应这种情况的方法。色觉缺陷通常是红绿色的,它是X连锁的反射性特征。主要是纯合子导致色觉缺陷。女性杂合子通常视力正常。色觉缺陷也有很强的遗传成分,尤其是如果父母都有色觉缺陷,而且有特定血型,而且近视或远视,他们的孩子很有可能是一样的。色盲通常在很小的时候就很明显了,当时孩子们正在学习自己的颜色,但却没有被发现,因为随着他们的成长,他们学会了将特定的颜色与某些物体联系起来。例如,他们知道草是绿色的,所以他们把看到的颜色叫做绿色。如果症状非常轻微,一个人可能没有意识到他们看不到某些颜色。
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