2 Fuchs' endothelial Corneal dystrophy

Also Known As:

Corneal dystrophy, Fuchs' endothelial, 2; Corneal Dystrophy, Fuchs Endothelial, 2; Corneal dystrophy, Fuchs' endothelial, late-onset; FECD2; Fuchs' endothelial corneal dystrophy 2; Late-onset Fuchs' endothelial corneal dystrophy

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Eye Diseases: 3522
- Corneal Diseases: 916
  - Hereditary Corneal Dystrophies: 820
    - Fuchs' Endothelial Dystrophy: 754
      - 2 Fuchs' endothelial Corneal dystrophy: 2
- Hereditary Eye Diseases: 18
  - Hereditary Corneal Dystrophies: 820
    - Fuchs' Endothelial Dystrophy: 754
      - 2 Fuchs' endothelial Corneal dystrophy: 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Eye Diseases: 18
    - Hereditary Corneal Dystrophies: 820
      - Fuchs' Endothelial Dystrophy: 754
        2 Fuchs' endothelial Corneal dystrophy: 2

Related Diseases

1.	Hereditary Corneal Dystrophies
2.	Corneal dystrophy and perceptive deafness

Experts

1.	Casey, Joseph: 1 article (02/2012)
2.	Loganathan, Sampath K: 1 article (02/2012)
3.	Quon, Anita: 1 article (02/2012)
4.	Sundaresan, Periasamy: 1 article (02/2012)
5.	Vilas, Gonzalo L: 1 article (02/2012)
6.	Vithana, Eranga N: 1 article (02/2012)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to 2 Fuchs' endothelial Corneal dystrophy:

1.	ThymineIBA 02/11/2023 - "Late-onset Fuchs endothelial corneal dystrophy (FECD) is a disease affecting the corneal endothelium (CE), associated with a cytosine-thymine-guanine repeat expansion at the CTG18.1 locus in the transcription factor 4 (TCF4) gene. "
2.	GuanineIBA 02/11/2023 - "Late-onset Fuchs endothelial corneal dystrophy (FECD) is a disease affecting the corneal endothelium (CE), associated with a cytosine-thymine-guanine repeat expansion at the CTG18.1 locus in the transcription factor 4 (TCF4) gene. "
3.	CytosineIBA 02/11/2023 - "Late-onset Fuchs endothelial corneal dystrophy (FECD) is a disease affecting the corneal endothelium (CE), associated with a cytosine-thymine-guanine repeat expansion at the CTG18.1 locus in the transcription factor 4 (TCF4) gene. "
4.	BoratesIBA 02/01/2012 - "Mutations in the SLC4A11 gene, which encodes a plasma membrane borate transporter, cause recessive congenital hereditary endothelial corneal dystrophy type 2 (CHED2), corneal dystrophy and perceptive deafness (Harboyan syndrome), and dominant late-onset Fuchs endothelial corneal dystrophy (FECD). "
5.	Transcription Factor 4IBA 02/11/2023 - "Late-onset Fuchs endothelial corneal dystrophy (FECD) is a disease affecting the corneal endothelium (CE), associated with a cytosine-thymine-guanine repeat expansion at the CTG18.1 locus in the transcription factor 4 (TCF4) gene. "