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

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Article

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

Vestnik oftalmologii - 1 Jan 2000

Petraevskiĭ A V

Abstract excerpt

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.

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PMID: 23210347

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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