Edict syndrome

Common Name(s)

Edict syndrome

EDICT syndrome is an autosomal dominant syndromal anterior segment dysgenesis characterized by endothelial dystrophy, iris hypoplasia, congenital cataract, and thinning of the corneal stroma ({9:Iliff et al., 2012}). Syndromes with overlapping features have been reported, including cornea guttata with anterior polar cataracts ({121390}) and congenital corneal opacities, cornea guttata, and corectopia ({608484}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Edict syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Edict syndrome" returned 1 free, full-text research articles on human participants. First 3 results:

A single-base substitution in the seed region of miR-184 causes EDICT syndrome.
 

Author(s): Benjamin W Iliff, S Amer Riazuddin, John D Gottsch

Journal:

 

To investigate the cause of the syndrome characterized by endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (EDICT).

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Edict syndrome" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.