Rieger’s Anomaly without Posterior Embryotoxon: A Rare Presentation
Rieger’s anomaly is a rare congenital ocular defect with autosomal dominant inheritance, characterised by dysgenesis of the anterior segment. Ocular features of typical Reiger’s anomaly include a prominent anteriorly displaced Schwalbe's line (posterior embryotoxon), iris stromal hypoplasia,...
| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | English |
| Publicado em: |
JCDR Research and Publications Private Limited
2020-12-01
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| Colecção: | Journal of Clinical and Diagnostic Research |
| Assuntos: | |
| Acesso em linha: | https://jcdr.net/articles/PDF/14335/45906_CE[Ra1]_F(KM)_PF1(ShG_SL)_PFA(SL)_PN(SL).pdf |