Prophylactic immunoglobulin therapy for pediatric congenital myotonic dystrophy

AbstractCongenital Myotonic Dystrophy (CMD) is an autosomal dominant hereditary disease caused by mutations in the dystrophia myotonica protein kinase gene. Patients with CMD often exhibit low immunoglobulin (Ig) G levels. While Ig replacement therapy for low IgG levels has been reported in several...

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Bibliographic Details
Main Authors: Yoji Uejima, Satoshi Sato
Format: Article
Language:English
Published: Taylor & Francis Group 2024-04-01
Series:Immunological Medicine
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/25785826.2024.2306672