Rhegmatogenous Retinal Detachment with Spontaneous Dialysis of the Ora Serrata in Neurofibromatosis Type 1: A Case Report

Neurofibromatosis type 1 is a genetic disorder that follows an autosomal dominant pattern of inheritance. Ocular involvement is not uncommon, but spontaneous dialysis of the retina in the absence of a history of trauma is a rare clinical entity. Rare cases of retinal involvement such as retinal deta...

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Detalles Bibliográficos
Autores principales: Shrestha, Richa Makaju, Bhatt, Swechha, Shrestha, Pooja, Sapkota, Prakash, Keshari, Rajani, Manandhar, Anu, Bhattarai, Iwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of the Nepal Medical Association 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9275462/
https://www.ncbi.nlm.nih.gov/pubmed/35690984
http://dx.doi.org/10.31729/jnma.7392

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9275462/
https://www.ncbi.nlm.nih.gov/pubmed/35690984
http://dx.doi.org/10.31729/jnma.7392

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