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Vestn Oftalmol. 2012 Sep-Oct;128(5):39-42.

[Familial case of Axenfeld anomaly associated with Shtargardt dystrophy].

[Article in Russian]

Abstract

A clinical case of Axenfeld anomaly (posterior embryotoxon) in a 3-generation family is presented. However mother and father are not related to each other. A son who had the most prominent clinical manifestation had a typical bilateral Shtargardt dystrophy.

PMID:
23210347
[Indexed for MEDLINE]
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