Bilateral Adduction Palsy in a Patient with Myotonic Dystrophy Type 1

Myotonic dystrophy type 1 (DM1) is caused by CTG repeat expansion in the DMPK gene in chromosome 19q13.3. External ophthalmoplegia is a rare manifestation in DM1. We report a DM1 patient confirmed by the presence of 650 CTG triplet expansions in the DMPK gene and had limitation of adduction gaze bil...

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Detalles Bibliográficos
Autores principales: Kim, Hong-Jeon, Oh, Jung-Hwan, Kang, Sa-Yoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923359/
https://www.ncbi.nlm.nih.gov/pubmed/27358583
http://dx.doi.org/10.5607/en.2016.25.3.143

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923359/
https://www.ncbi.nlm.nih.gov/pubmed/27358583
http://dx.doi.org/10.5607/en.2016.25.3.143

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