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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Detalles Bibliográficos
Autores principales: Gołaszewska, Kinga, Dub, Natalia, Saeed, Emil, Mariak, Zofia, Konopińska, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008669/
https://www.ncbi.nlm.nih.gov/pubmed/33781219
http://dx.doi.org/10.1186/s12886-021-01899-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008669/
https://www.ncbi.nlm.nih.gov/pubmed/33781219
http://dx.doi.org/10.1186/s12886-021-01899-2

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