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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2022
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| Materias: | |
| 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 |