A comparative analysis of clinical phenotypes and outcomes in childhood interstitial lung disease due to surfactant dysfunction disorders: focusing on mutations in SFTPC, ABCA3, and NKX2-1 genes
Abstract Background Surfactant dysfunction disorders are a group of rare diseases that lead to childhood interstitial lung diseases (ILD). SFTPC, ABCA3, and NKX2-1 are the three genetic forms of this condition. The differences in clinical presentations and prognostic outcomes across these genotypes...
שמור ב:
| Principais autores: | , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMC
2025-08-01
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| סדרה: | Italian Journal of Pediatrics |
| נושאים: | |
| גישה מקוונת: | https://doi.org/10.1186/s13052-025-02110-8 |
| תגים: |
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