Hypogammaglobulinemia and infection risk in myotonic dystrophy type 1

IgG deficiency is a frequent occurrence in DM1 patients and is associated with CTG repeat expansion size. Whether hypogammaglobulinemia is associated with increased infection risk in DM1 is unclear. A prospective multicenter cohort study is needed to evaluate this.

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Publication Details

Journal
Muscle & Nerve
Published
2024-09-12
DOI
https://doi.org/10.1002/mus.28247
Citations
2
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.54
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article

Hypogammaglobulinemia and infection risk in myotonic dystrophy type 1

Sandhya Limaye, Shadi El‐Wahsh, Katrina Morris, Sean Riminton et al.
2 citations
Muscle & Nerve
Genetic Neurodegenerative Diseases
0.54
article

Hypogammaglobulinemia and infection risk in myotonic dystrophy type 1

Sandhya Limaye, Shadi El‐Wahsh, Katrina Morris, Sean Riminton, Alastair Corbett, James Triplett
article en
2 citations

Abstract

IgG deficiency is a frequent occurrence in DM1 patients and is associated with CTG repeat expansion size. Whether hypogammaglobulinemia is associated with increased infection risk in DM1 is unclear. A prospective multicenter cohort study is needed to evaluate this.

Muscle & NerveVol. 70(5)
The University of Sydney (AU), Concord Repatriation General Hospital (AU), UNSW Sydney (AU), South Western Sydney Local Health District (AU)
Good health and well-being
Openalex Percentile: Top 35%
Genetic Neurodegenerative Diseases
0.54
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