Achromatopsia: meaning, definitions and examples

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achromatopsia

 

[ รฆหŒkroสŠmษ™หˆtษ‘หpziษ™ ]

Noun
Context #1 | Noun

vision disorder

Achromatopsia is a rare vision disorder characterized by the absence of color vision. Individuals with this condition see the world in shades of gray or black and white. It results from the malfunctioning of the cone cells in the retina, which are responsible for color perception.

Examples of usage

  • Achromatopsia affects an individual's ability to distinguish colors.
  • People with achromatopsia may experience difficulties in bright light.
  • Achromatopsia can lead to significant challenges in daily life due to reduced visual information.
  • Research is ongoing to better understand and potentially treat achromatopsia.

Translations

Translations of the word "achromatopsia" in other languages:

๐Ÿ‡ต๐Ÿ‡น acromatopsia

๐Ÿ‡ฎ๐Ÿ‡ณ เค…เค•เฅเคฐเฅ‹เคฎเฅˆเคŸเฅ‹เคชเฅเคธเคฟเคฏเคพ

๐Ÿ‡ฉ๐Ÿ‡ช Achromatopsie

๐Ÿ‡ฎ๐Ÿ‡ฉ akromatopsia

๐Ÿ‡บ๐Ÿ‡ฆ ะฐั…ั€ะพะผะฐั‚ะพะฟัั–ั

๐Ÿ‡ต๐Ÿ‡ฑ akromatopsja

๐Ÿ‡ฏ๐Ÿ‡ต ใ‚ขใ‚ฏใƒญใƒžใƒˆใƒ—ใ‚ทใƒผ

๐Ÿ‡ซ๐Ÿ‡ท achromatopsie

๐Ÿ‡ช๐Ÿ‡ธ acromatopsia

๐Ÿ‡น๐Ÿ‡ท akromatopsi

๐Ÿ‡ฐ๐Ÿ‡ท ๋ฌด์ฑ„์ƒ‰์ฆ

๐Ÿ‡ธ๐Ÿ‡ฆ ุงู†ุนุฏุงู… ุงู„ุฃู„ูˆุงู†

๐Ÿ‡จ๐Ÿ‡ฟ achromatopsie

๐Ÿ‡ธ๐Ÿ‡ฐ achromatopsia

๐Ÿ‡จ๐Ÿ‡ณ ๆ— ่‰ฒ่ง†็—‡

๐Ÿ‡ธ๐Ÿ‡ฎ akromatopsija

๐Ÿ‡ฎ๐Ÿ‡ธ akromatopsรญa

๐Ÿ‡ฐ๐Ÿ‡ฟ ะฐั…ั€ะพะผะฐั‚ะพะฟัะธั

๐Ÿ‡ฌ๐Ÿ‡ช แƒแƒฅแƒ แƒแƒ›แƒแƒขแƒแƒžแƒกแƒ˜แƒ

๐Ÿ‡ฆ๐Ÿ‡ฟ akromatopsiya

๐Ÿ‡ฒ๐Ÿ‡ฝ acromatopsia

Etymology

The term 'achromatopsia' comes from the Greek roots 'a-' meaning 'without,' 'chroma' meaning 'color,' and 'opsia' meaning 'sight' or 'vision.' The word reflects the condition's defining characteristic: the absence of color vision. Achromatopsia is associated with defects in the cone photoreceptors in the retina, which are responsible for detecting color, and it can be inherited as an autosomal recessive trait. The condition was first described in medical literature in the late 19th century, but its understanding has evolved significantly with advances in genetics and ophthalmology. Researchers continue to explore the genetic underpinnings and possible treatment options for individuals affected by this disorder.