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Identification of Gene Mutations in Atypical Retinopathy of Prematurity Cases
PURPOSE: We have observed that some preterm infants whose fundus appears very similar to eyes with familial exudative vitreoretinopathy (FEVR) present with atypical retinopathy of prematurity (ROP). To establish a definitive diagnosis and explore the possible genetic mechanism of atypical ROP, we pe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455826/ https://www.ncbi.nlm.nih.gov/pubmed/32884843 http://dx.doi.org/10.1155/2020/4212158 |