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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...
Autores principales: | Shrestha, Richa Makaju, Bhatt, Swechha, Shrestha, Pooja, Sapkota, Prakash, Keshari, Rajani, Manandhar, Anu, Bhattarai, Iwa |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Journal of the Nepal Medical Association
2022
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Materias: | |
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 |
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