Caricamento...
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...
Salvato in:
| Pubblicato in: | Am J Ophthalmol Case Rep |
|---|---|
| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2020
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7260431/ https://ncbi.nlm.nih.gov/pubmed/32490286 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajoc.2020.100753 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|