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A rare case of neurofibromatosis type I with unilateral congenital ectropion uveae and glaucoma
PURPOSE: Neurofibromatosis Type I (NF-1) is a neurocutaneous disease affecting the skin, eye and peripheral nervous system. Congenital glaucoma is a rare association, but can be a prelude to the diagnosis of NF-1 later in life. We report this unusual association in a child and discuss the possible u...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260431/ https://www.ncbi.nlm.nih.gov/pubmed/32490286 http://dx.doi.org/10.1016/j.ajoc.2020.100753 |