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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| Principais autores: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis Group
2024-04-01
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| coleção: | Immunological Medicine |
| Assuntos: | |
| Acesso em linha: | https://www.tandfonline.com/doi/10.1080/25785826.2024.2306672 |
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