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Axenfeld‐Rieger syndrome combined with a foveal anomaly in a three‐generation family: a case report
BACKGROUND: Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant eye disorder that can also affect other organs of the human body. The condition is primarily characterized by the anterior segmental abnormalities of the eye. Here, we present an observational case series of a three-generation f...
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| Publicado no: | BMC Ophthalmol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8008669/ https://ncbi.nlm.nih.gov/pubmed/33781219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12886-021-01899-2 |
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