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...

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Detalles Bibliográficos
Autores principales: Venkataraman, Prasanna, Manapakkam, Madhuri, Mohan, Neethu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
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

Internet

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

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