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Two cases of myotonic dystrophy manifesting various ophthalmic findings with genetic evaluation
We report two cases of myotonic dystrophy in one family; both diagnosed from genetic analysis following ophthalmic indications, but before the manifestation of systemic symptoms. A 39-year-old female visited our clinic for routine examination. Mild ptosis, sluggish pupillary response, and bilateral...
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| Publicado no: | Indian J Ophthalmol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5026082/ https://ncbi.nlm.nih.gov/pubmed/27609169 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0301-4738.190157 |
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