Add to ORKGColor blindness or color vision deficiency is X-linked recessive disorder that affects males more frequently than females. Abnormality in any one or all three cone photoreceptors caused Congenital disorders. Protanopia, deuteranopia results when long wavelength (L), photopigments (red), middle wavelength (M) and photopigments (green) are missing. This cross-sectional study was done to find out the prevalence of color vision deficiency among basic school students in Koya city with different ages and genders. The study was conducted in four basic schools that were present in Koya city (Zheen, Zanst, Nawroz and Najibaxan). All students screened by using Ishihara 24 plates. For the study (n=400, male=206, female=194, age=8-14) were select...
AbstractX-linked red–green color blindness is the most widespread form of vision impairment. The stu...
Background: Color vision deficiency is an X-linked recessive condition. This is more common among ma...
Background: Color vision deficiency (CVD) is an X chromosome-linked recessive autosomal dominant. De...
Color blindness or color vision deficiency is X-linked recessive disorder that affects males more fr...
Color vision deficiency is a condition affecting human's ability to see or recognize specific colors...
Background and aims: Color blindness is a disease that remains undiagnosed in some cases. The diagn...
Background: Congenital colour vision defects are x-linked inherited, non-progressive and untreatable...
AbstractX-linked red–green color blindness is the most widespread form of vision impairment. The stu...
Introduction: Due to the importance of color blindness and its impact on the depth and quality...
INTRODUCTION: Color vision defect can be observed in various diseases of optic nerve and retina and ...
Introduction: Color blindness is X-linked recessive inherited disorder that occurs mostly in males a...
Background: Congenital colour vision defects are x-linked inherited, non-progressive and untreatable...
Color blindness (color vision deficiency) is a disorder that impairs the true perception of colors. ...
Introduction: Colour vision deficiency is a common ocular disorder, but it often goes unnoticed due ...
Background: Color vision deficiency is an X-linked recessive condition. This is more common among ma...
AbstractX-linked red–green color blindness is the most widespread form of vision impairment. The stu...
Background: Color vision deficiency is an X-linked recessive condition. This is more common among ma...
Background: Color vision deficiency (CVD) is an X chromosome-linked recessive autosomal dominant. De...
Color blindness or color vision deficiency is X-linked recessive disorder that affects males more fr...
Color vision deficiency is a condition affecting human's ability to see or recognize specific colors...
Background and aims: Color blindness is a disease that remains undiagnosed in some cases. The diagn...
Background: Congenital colour vision defects are x-linked inherited, non-progressive and untreatable...
AbstractX-linked red–green color blindness is the most widespread form of vision impairment. The stu...
Introduction: Due to the importance of color blindness and its impact on the depth and quality...
INTRODUCTION: Color vision defect can be observed in various diseases of optic nerve and retina and ...
Introduction: Color blindness is X-linked recessive inherited disorder that occurs mostly in males a...
Background: Congenital colour vision defects are x-linked inherited, non-progressive and untreatable...
Color blindness (color vision deficiency) is a disorder that impairs the true perception of colors. ...
Introduction: Colour vision deficiency is a common ocular disorder, but it often goes unnoticed due ...
Background: Color vision deficiency is an X-linked recessive condition. This is more common among ma...
AbstractX-linked red–green color blindness is the most widespread form of vision impairment. The stu...
Background: Color vision deficiency is an X-linked recessive condition. This is more common among ma...
Background: Color vision deficiency (CVD) is an X chromosome-linked recessive autosomal dominant. De...