n.（全）色盲

Achromatopsia is a rare genetic disorder that causes complete lack of color vision.
这是一种罕见的遗传性疾病，会导致完全丧失色觉。
The patient was diagnosed with achromatopsia after extensive eye tests.
在进行了详细的视力检查后，病人被诊断为患有色盲症。
Achromatopsia is characterized by the inability to distinguish between colors, making everyday tasks challenging.
色盲症的特征是无法区分颜色，这使得日常任务变得困难重重。
The child's world is filled with grayscale due to their early onset of achromatopsia.
由于早期患上色盲症，这个孩子的世界充满了灰度。
Scientists have been studying the neural mechanisms of achromatopsia in an effort to develop treatments.
科学家们正在研究色盲症的神经机制，以期找到治疗方法。
Individuals with achromatopsia often rely on other senses, like touch and sound, to navigate their environment.
患有色盲症的人通常会依赖触觉和听觉来感知环境。
Hereditary achromatopsia can be inherited from one parent who is a carrier of the mutated gene.
遗传性色盲症可能由携带突变基因的一方遗传给下一代。
Achromatopsia affects not just visual perception but also spatial awareness and navigation.
色盲症不仅影响视觉感知，还会影响空间意识和导航能力。
Artists with achromatopsia often create striking works, focusing on texture and form rather than color.
色盲的艺术家常常创作出引人注目的作品，他们更注重纹理和形态而非色彩。
Novel therapies, such as gene therapy, are being explored to potentially cure or manage the symptoms of achromatopsia.
新的疗法，如基因疗法，正在被探索以可能治愈或管理色盲症的症状。