| Autor: |
Cennamo, Gilda, Montorio, Daniela, Paola Laezza, Maria, Giunta, Piera, Barra, Pasquale Fabio, Scala, Iris |
| Předmět: |
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| Zdroj: |
Acta Ophthalmologica (1755375X); Dec2021, Vol. 99 Issue 8, pe1537-e1539, 3p |
| Abstrakt: |
Fundus examination of all patients with OPG revealed the optic disc had oedema and a blurred margin, while no papillary alteration was detected in subjects without OPG. Neurofibromatosis type 1 (NF1) is an autosomal neurogenetic disorder, and its main clinical phenotype is the development of optic pathway gliomas (OPGs). Spectral-domain optical coherence tomography (SD-OCT), a rapid diagnostic tool, detects changes in the retinal ganglion cell complex (GCC), the retinal nerve fibre layer (RNFL) and their relationship to vision loss in patients with OPGs (Topcu-Yilmaz et al. 2014). [Extracted from the article] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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