Axenfeld‐Rieger syndrome combined with a foveal anomaly in a three‐generation family: a case report
Abstract 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-gene...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMC
2021-03-01
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| Sarja: | BMC Ophthalmology |
| Aiheet: | |
| Linkit: | https://doi.org/10.1186/s12886-021-01899-2 |
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