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Ocular findings associated with FADD deficiency resemble familial exudative vitreoretinopathy
PURPOSE: We report the first known case of eye findings associated with a Fas-associated protein with death domain (FADD) gene mutation, an exceedingly rare entity. OBSERVATIONS: A 7-year-old boy was referred for decreased vision and eye examination revealed cystoid macular edema and peripheral reti...
| 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/PMC8859737/ https://www.ncbi.nlm.nih.gov/pubmed/35243129 http://dx.doi.org/10.1016/j.ajoc.2022.101305 |