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Significados de achromatopsia en inglés
Human illness, a type of color blindness.
Términos relacionados
Sinónimos
Examples for "achromatism"
Examples for "achromatism"
1
He will find that he has not given exactly the proper curves to secure achromatism.
2
This artifice is specially adopted in objectives for astronomical photography (''pure actinic achromatism'').
3
Soc., 1878), the most suitable for visual instruments (''optical achromatism,').
4
The absence of this error is termed achromatism, and an optical system so corrected is termed achromatic.
5
As the diameter of the lens was so small in comparison with its focal length, its want of achromatism was inappreciable.
1
We have performed linkage analysis in eight families with rod monochromacy, an autosomal recessively inherited condition with complete color blindness.
2
This defines an interval of approximately 3 cM covering the ACHM2 locus for rod monochromacy.
3
Go into this then choose Simulate color space and Monochromacy to go gray.
1
Ryan is one of few critics who have consistently criticized television's monochromatism.
2
You were born with a condition called rod monochromatism.
3
In the other patients, either rod monochromatism or cone-rod dystrophy could not be excluded with certainty.
1
The vision in typical complete achromatopsia is mediated only by rods.
1
We have performed linkage analysis in eight families with rod monochromacy, an autosomal recessively inherited condition with complete color blindness.
1
We have performed linkage analysis in eight families with rod monochromacy, an autosomal recessively inherited condition with complete color blindness.
2
This defines an interval of approximately 3 cM covering the ACHM2 locus for rod monochromacy.
1
You were born with a condition called rod monochromatism.
2
In the other patients, either rod monochromatism or cone-rod dystrophy could not be excluded with certainty.
Uso de achromatopsia en inglés
1
Our results demonstrate that GNAT2 is the third gene implicated in achromatopsia.
2
We describe a patient with persistent cerebral achromatopsia occurring after bilateral occipital strokes.
3
The vision in typical complete achromatopsia is mediated only by rods.
4
Conclusion: We report the occurrence of CNGB3-achromatopsia in a new canine breed, the MAS.
5
Patients with cerebral achromatopsia are commonly said to suffer due to their disturbed colour sense.
6
Here we analyze the molecular basis of achromatopsia in two siblings with residual cone function.
7
Cerebral achromatopsia is a rare disorder of colour vision caused by bilateral damage to the occipito-temporal cortex.
8
Neil Harbisson has the condition achromatopsia, a hereditary vision disorder which affects one in 33,000 people.
9
Results: Here we report an in-depth characterization of the achromatopsia phenotype in a new canine breed, the miniature Australian shepherd (MAS).
10
A substantial number of foveal and parafoveal cone photoreceptors with apparently intact inner segments were identified in patients with the inherited disease achromatopsia.
11
In conclusion, mutations in the CNGB3 gene are responsible for approximately 50% of all patients with achromatopsia.
12
Here, we analyzed the spectrum and prevalence of CNGB3 gene mutations in a cohort of 341 independent patients with achromatopsia.
13
We here report the identification of five independent families with achromatopsia that segregate protein-truncation mutations in the GNAT2 gene, located on chromosome 1p13.
14
Achromatopsia is an autosomal recessively inherited visual disorder that is present from birth and that features the absence of color discrimination.
15
Achromatopsia is an inherited retinal disorder of cone photoreceptors characterized by markedly reduced visual acuity, extreme light sensitivity, and absence of color discrimination.
16
Our results demonstrate that GNAT2 is the third gene implicated in achromatopsia.
Sobre este término
Colocaciones frecuentes
Translations for achromatopsia
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Achromatopsia a través del tiempo