Congenital endothelial dystrophy type 2

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Congenital endothelial dystrophy type 2
Classification and external resources
File:Congenital hereditary endothelial dystrophy 1.JPEG
A markedly opaque cornea due to stromal edema secondary to defective endothelial cells (Courtesy of Dr. Ahmed A. Hidajat)
OMIM 217700

Congenital endothelial dystrophy type 2 is a rare form of human corneal dystrophy. It is associated with mutations in SLC4A11 gene.[1]

References

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See also

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ru:Врождённая эндотелиальная дистрофия роговицы, тип 2
Epithelial and Subepithelial
Epithelial basement membrane dystrophy (OMIM 121820), called a corneal dystrophy but in reality this condition is not inherited in the majority of cases, representing a non-specific reaction to a variety of corneal insults. · Subepithelial mucinous corneal dystrophy · Meesmann juvenile epithelial corneal dystrophy (MECD, Stocker-Holt dystrophy, OMIM 122100) · Lisch epithelial dystrophy · Gelatinous drop-like corneal dystrophy
Bowman layer
Reis-Bucklers corneal dystrophy (CDB1) aka. Granular corneal dystrophy type III · Thiel-Behnke dystrophy (CDB2)
Stroma
Descemet membrane and Endothelial

M: EYE

anat(g, a, p)/phys/devp/cell

proc, drug(S1A/1E/1F/1L)

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