Enhanced serum immunoglobulin G clearance in myotonic dystrophy-associated hypogammaglobulinemia: a case series and review of the literature

BACKGROUND: Myotonic dystrophy type 1 is an autosomal dominant disorder characterized by muscle weakness, myotonia, cataracts, and cardiac conduction defects; it is associated with expansions of cytosine-thymine-guanine repeats in the myotonic dystrophy protein kinase. Hypogammaglobulinemia is a les...

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Detalles Bibliográficos
Autores principales: Sasson, Sarah C., Corbett, Alastair, McLachlan, Andrew J., Chen, R., Adelstein, S. A., Riminton, Sean, Limaye, Sandhya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864924/
https://www.ncbi.nlm.nih.gov/pubmed/31744540
http://dx.doi.org/10.1186/s13256-019-2285-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864924/
https://www.ncbi.nlm.nih.gov/pubmed/31744540
http://dx.doi.org/10.1186/s13256-019-2285-3

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