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Antibody deficiency in myotonic dystrophy type 1: A differential diagnosis below the radar.

Created on 30 Sep 2026

Authors

Edoardo Galli, Christoph T Berger, Thomas Daikeler, Anne-Kathrin Peyer Kauffmann, Marc Emmenegger, Armin Droll, Andrea Egger, Michael Sinnreich, Mike Recher

Published in

Journal of human immunity. Volume 2. Issue 6. Nov 02, 2026. Epub Sep 30, 2026.

Abstract

Myotonic dystrophy type 1 is a rare, underdiagnosed genetic neuromuscular disorder that is often accompanied by hypogammaglobulinemia, serving as a crucial diagnostic clue. We report the clinical and immunophenotypic features of two patients and discuss the underlying pathogenesis.

PMID:
42814028
Bibliographic data and abstract were imported from PubMed on 30 Sep 2026.

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