University of Iowa Health Care

Ophthalmology and Visual Sciences

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Avellino Dystrophy

Contributor:  Caroline W. Wilson, MD and Mark A. Greiner, MD

Photographer:  Brice Critser, CRA

Category(ies): Cornea / External Eye Disease

Posted June 24, 2019

This 23-year-old female patient has granular type II (Avellino) corneal dystrophy and recurrent erosions. She has a strong family history of this autosomal dominant corneal dystrophy.  In both eyes, there are linear lattice deposits and granular deposits in the central and paracentral anterior stroma with clear intervening stroma between the deposits. The right eye (top) has undergone phototherapeutic keratectomy and exhibits diffuse subepithelial haze. Treatment for her recurrent erosions included ocular surface lubrication with preservative-free artificial tears, sodium chloride 5% ointment, and rigid gas-permable contact lenses.


Avellino Dystrophy: Type II granular corneal dystrophy

Contributor: Matthew Ward, MD, The University of Iowa

Category: Cornea

Posted September 21, 2012

Avellino Dystrophy

a closer look at the above with a slit lamp

47-year-old man with type II granular corneal dystrophy (Avellino) manifested after undergoing LASIK vision correction. Avellino dystrophy is known to blossom after LASIK. For this reason, it is the practice in some Asian countries with high prevalence of Avellino (most prominently Korea where prevalence approaches 1/1000) to perform routine genetic testing to rule out the TGF beta 1 mutation in all candidates for laser vision correction. For more information on the anterior stromal corneal dystrophies see the following case: Epithelial-Stromal and Stromal Corneal Dystrophies


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last updated: 09/21/2012; updated 6/24/2019
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