A Case of Myotonic Dystrophy with Electrolyte Imbalance

Type 1 myotonic dystrophy (DM1) is an autosomal-dominant inherited disorder with a multisystem involvement, caused by an abnormal expansion of the CTG sequence of the dystrophic myotonia protein kinase (DMPK) gene. DM1 is a variable multisystem disorder with muscular and nonmuscular abnormalities. I...

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Detalles Bibliográficos
Autores principales: Ko, Weon-Jin, Kim, Kwang-Yeol, Kim, So-Mi, Hong, Seung-Jae, Lee, Sang-Hoon, Song, Ran, Yang, Hyung-In, Lee, Yeon-Ah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708088/
https://www.ncbi.nlm.nih.gov/pubmed/23853500
http://dx.doi.org/10.3346/jkms.2013.28.7.1111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708088/
https://www.ncbi.nlm.nih.gov/pubmed/23853500
http://dx.doi.org/10.3346/jkms.2013.28.7.1111

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