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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Autors principals:	Yoji Uejima, Satoshi Sato
Format:	Artigo
Idioma:	Inglês
Publicat:	Taylor & Francis Group 2024-04-01
Col·lecció:	Immunological Medicine
Matèries:	Hypogammaglobulinemia pediatric congenital myotonic dystrophy intravenous immunoglobulins subcutaneous immunoglobulins neonatal fc receptor
Accés en línia:	https://www.tandfonline.com/doi/10.1080/25785826.2024.2306672
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