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Neurofibromatosis Type-2 presenting with vision impairment
Neurofibromatosis Type-2 (NF2) is an autosomal dominant genetic tumour-predisposing condition caused by mutations in the NF2 gene located on chromosome 22q12. It is characterized by multiple benign tumours of the central and peripheral nervous systems and meninges, causing high morbidity. Herein, pr...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Professional Medical Publications
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10025740/ https://www.ncbi.nlm.nih.gov/pubmed/36950434 http://dx.doi.org/10.12669/pjms.39.2.6813 |