Novel retinal observations in a child with DiGeorge (22q11.2 deletion) syndrome

PURPOSE: DiGeorge (22q11.2 deletion) syndrome is the most common human deletion syndrome with wide range of ocular manifestations. Herein we describe a case with novel retinal observations in this conditions. OBSERVATIONS: Retinal vascular dysplasia, peripapillary, intraretinal and vitreous hemorrha...

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Detalles Bibliográficos
Autores principales: Kozak, Igor, Ali, Syed A., Wu, Wei-Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184887/
https://www.ncbi.nlm.nih.gov/pubmed/35692436
http://dx.doi.org/10.1016/j.ajoc.2022.101608

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184887/
https://www.ncbi.nlm.nih.gov/pubmed/35692436
http://dx.doi.org/10.1016/j.ajoc.2022.101608

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