Corneal dystrophy, gelatinous drop-like

*Gene map locus 1p32

Amyloid corneal dystrophy, Japanese type

Amyloidosis, corneal

CDGDL

Corneal dystrophy, lattice type III

GDLD

Lattice corneal dystrophy, type III

[Clinical features: corneal dystrophy; central raised gelatinous, mulberry-shaped corneal masses; cataracts]

[Inheritance: autosomal recessive]

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Apolipoproteins J and E co-localise with amyloid in gelatinous drop-like and lattice type I corneal dystrophies	Presence of vitronectin in neovascularised cornea of patient with gelatinous drop-like dystrophy	Presence of vitronectin in neovascularised cornea of patient with gelatinous drop-like dystrophy
British Journal of Ophthalmology	British Journal of Ophthalmology	British Journal of Ophthalmology


Gelatinous drop-like corneal dystrophy in a child with developmental delay: clinicopathological features and exclusion of the M1S1 gene	Gelatinous drop-like corneal dystrophy in a child with developmental delay: clinicopathological features and exclusion of the M1S1 gene	Lattice corneal dystrophy type III with corneal fistula. A case report
Eye	Eye	Indian Journal of Ophthalmology


Lattice corneal dystrophy type III with corneal fistula. A case report	Lattice corneal dystrophy type III with corneal fistula. A case report	Four Mutations (Three Novel, One Founder) in TACSTD2 among Iranian GDLD Patients
Indian Journal of Ophthalmology	Indian Journal of Ophthalmology	Investigative Ophthalmology & Visual Science


Phenotypic Investigation of Cell Junction-Related Proteins in Gelatinous Drop-Like Corneal Dystrophy	Phenotypic Investigation of Cell Junction-Related Proteins in Gelatinous Drop-Like Corneal Dystrophy	A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy
Investigative Ophthalmology & Visual Science	Investigative Ophthalmology & Visual Science	Molecular Vision


A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy	A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy	A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy
Molecular Vision	Molecular Vision	Molecular Vision

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Edited by Aldo Campana, August 21, 2012