A new ABCA3 Gene Mutation Presenting as Early Neonatal Surfactant Deficiency
Interstitial lung disease is a very heterogeneous group of diseases. Dysfunction of surfactant proteins is included in this group and ABCA3 gene mutations are a well-established genetic cause. There is a large spectrum of clinical presentation concerning ABCA3 mutations ranging from neonatal early...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Sociedade Portuguesa de Pediatria
2021-07-01
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| Series: | Portuguese Journal of Pediatrics |
| Online Access: | https://pjp.spp.pt/article/view/20929 |