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The rare Axenfeld–Rieger syndrome with systemic anomalies: A case report and brief review of literature
RATIONALE: Axenfeld–Rieger syndrome (ARS) is a rare autosomal dominant disorder with ocular anterior segment dysgenesis and systemic anomalies. PATIENT CONCERNS: A 28-year-old Chinese Han female was referred to Beijing Tongren Eye Center for progressive decrease of the visual acuity on her right eye...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Wolters Kluwer Health
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571701/ https://www.ncbi.nlm.nih.gov/pubmed/28816964 http://dx.doi.org/10.1097/MD.0000000000007791 |