amaurosis in English

noun
1
partial or total blindness without visible change in the eye, typically due to disease of the optic nerve, spinal cord, or brain.
Leber congenital amaurosis is an inherited disease that is believed to cause up to 20 percent of all cases of childhood blindness.

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Below are sample sentences containing the word "amaurosis" from the English Dictionary. We can refer to these sentence patterns for sentences in case of finding sample sentences with the word "amaurosis", or refer to the context using the word "amaurosis" in the English Dictionary.

1. Amaurosis fugax synonyms, Amaurosis fugax pronunciation, Amaurosis fugax translation, English dictionary definition of Amaurosis fugax

2. What are synonyms for Amaurosis?

3. Synonyms for Amaurosis in Free Thesaurus

4. Amaurosis >> Leber congenital Amaurosis (LCA) is an inherited disease which usually causes total blindness from birth

5. Amaurosis congenita of Leber, amaurosis fugax, amaurotic pupil, amaut, amaze, Amazeballs, amazed, amazement, amazia, Amaziah, amazing

6. Mutations to the RPE65 can cause Leber Amaurosis

7. Amaurosis conge´nita (Amaurosis congenita of Leber) (congenital Amaurosis) hereditary blindness occurring at or shortly after birth, associated with an atypical form of diffuse pigmentation and commonly with optic atrophy

8. Amaurotic (not comparable) Pertaining to or suffering from amaurosis

9. What is Leber Congenital Amaurosis? Leber congenital Amaurosis (LCA) is a group of inherited retinal diseases characterized by severe impairment vision or blindness at birth

10. 613826 - LEBER CONGENITAL Amaurosis 6; LCA6 Dryja et al

11. We will discuss various aetiologies of Amaurosis and its treatment.

12. Leber congenital Amaurosis (LCA) is a rare genetic eye disorder

13. Definition of Amaurosis : partial or complete loss of sight occurring especially without an externally perceptible change in the eye Other Words from Amaurosis Example Sentences Learn More about …

14. Leber congenital Amaurosis (LCA) is an eye disorder that primarily affects the retina

15. 4 words related to Amaurosis: vision defect, visual defect, visual disorder, visual impairment

16. Leber congenital Amaurosis is a congenital retinal dystrophy described almost 150 years ago

17. Most people chose this as the best definition of Amaurotic: Pertaining to amaurosis

18. Amaurosis fugax (from the Greek "Amaurosis," meaning dark, and the Latin "fugax," meaning fleeting) refers to a transient loss of vision in one or both eyes [ 1 ]

19. Leber Congenital Amaurosis (LCA) Treatments Scientists have identified multiple genetic mutations that can cause LCA

20. Amaurotic: [ am″aw-rot´ik ] pertaining to, or of the nature of, amaurosis

21. ‘Leber congenital Amaurosis is an inherited disease that is believed to cause up to 20 percent of all cases of childhood blindness.’ More example sentences ‘Other visual symptoms may include Amaurosis fugax, diplopia and partial loss of vision.’

22. Amaurosis a condition of partial or total blindness, caused by a disease of the optie nerve

23. Amaurosis fugax is sudden, temporary vision loss due to a lack of blood reaching the eye

24. Leber congenital Amaurosis (LCA) is a rare type of inherited eye disorder that causes severe vision loss at birth

25. The operation should be carried out within 24 h of onset of the deterioration of vision or amaurosis.

26. -It had a RPEG5 gene and was blind (Leber Amaurosis) -Person mostly related to dog than mouse

27. Amaurosis fugax happens when one of these clots gets stuck in an eye artery for a short time

28. Amaurosis Fugax is the temporary loss of vision in one eye due to the absence of blood circulation to the retina

29. Amaurosis is a paralysis of the nerves of the eye: it is sometimes cured, but then gradually, and not instantaneously

30. Today, Leber congenital Amaurosis is proving instrumental in our understanding of the molecular events that determine normal and aberrant retinal development

31. Leber congenital amaurosis (LCA) usually describes patients with severely reduced vision due to a retinal dystrophy in early childhood.

32. In the female patient, the acute amaurosis of the left eye pointed to an involvment of the ophthalmic artery.

33. Nonvascular ophthalmi an neurologid c c disorders that can be confused with Amaurosis fugax are listed, an and algorithm for evaluation

34. Leber congenital Amaurosis (LCA) is the most severe retinal dystrophy causing blindness or severe visual impairment before the age of 1 year

35. We report on an externally treated patient with amaurosis fugax due to postinterventional distal kinking and a primary residual stenosis.

36. Amaurosis fugax is a temporary loss of vision in one or both eyes due to a lack of blood flow to the retina

37. The visual impairment tends to be stable, although it may worsen very slowly over time.Leber congenital Amaurosis is also associated

38. Leber congenital Amaurosis (LCA) is a rare inherited eye disease that appears at birth or in the first few months of life.

39. Amaurosis [am″aw-ro´sis] loss of sight without apparent lesion of the eye, as from disease of the optic nerve, spine, or brain

40. Amaurosis is an organic loss of visual acuity which can attain blindness and which occurs suddenly in the absence of other ophthalmological changes

41. Amaurosis fugax is a temporary loss of vision in one or both eyes due to a lack of blood flow to the retina

42. Here, it is necessary to take into account the degree of stenosis, an initial clinical symptom (amaurosis fugax, TIA, stroke), and postoperative risk.

43. Contraindications are lesions of the bulbus oculi and the fundus, lesions of the chiasma opticum and a posttraumatic amaurosis caused by a sinus-cavernosus-fistula.

44. Results: Indications for CEA were asymptomatic carotid stenosis (40.6%), transient ischemic attack (TIA) or amaurosis fugax (AF, 39.9%), acute/progressive stroke (5%), and minor stroke (14.1%).

45. Why is it a mistake to call RPE65 "the Leber Amaurosis gene"? The RPE65 gene is 99.99% for protein for eye-sight

46. The trial, which was partly funded by the EU, involves adults and children who have an inherited retinal disease called Leber's congenital amaurosis (LCA).

47. The purpose of this study is to learn about a new gene therapy for patients with Leber Congenital Amaurosis caused by the CEP290 mutation

48. In 4 patients the vision returned completely after operation, 1 patient showed only a partial improvement and in 3 cases the amaurosis remained unchanged.

49. A visual impairment occurs in about 50% of patients with giant cell arteritis (GCA), an amaurosis fugax (AF) in about 30%, and diplopia in about 10%.

50. Among the etiological variety of types of post-traumatic amaurosis, this rare cause should be taken into consideration in the etiology, diagnosis and therapy, if appropriate.