congenital amaurosis in Vietnamese

Mù bẩm sinh

Sentence patterns related to "congenital amaurosis"

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

1. 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

2. 613826 - LEBER CONGENITAL Amaurosis 6; LCA6 Dryja et al

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

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

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

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

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

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

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

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

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

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

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

14. 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).

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

16. (2001) surveyed 57 unrelated patients who had Leber congenital Amaurosis for mutations in RPGRIP1 and found recessive mutations involving both alleles in 3 (6%) patients

17. Epidemiology Leber congenital Amaurosis (LCA) is the second most common group of inherited retinal dystrophies after retinitis pigmentosa, accounting for about 5% of all retinal dystrophies

18. From GHR Leber congenital Amaurosis is an eye disorder that primarily affects the retina, which is the specialized tissue at the back of the eye that detects light and color

19. Collapse Section Leber congenital Amaurosis is an eye disorder that primarily affects the retina, which is the specialized tissue at the back of the eye that detects light and color

20. 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

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.’