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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...

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Detalles Bibliográficos
Autores principales: Song, Wei, Hu, Xiaodan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
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