A rare interstitial lung disease in young adulthood due to surfactant protein C gene mutation: Two case reports with brief literature review

Interstitial lung disease associated with mutations in the surfactant protein C gene (SFTPC) is a rare condition. These mutations can be inherited as an autosomal dominant trait or occur sporadically due to a de novo mutation. The clinical symptoms of this disease can vary widely, ranging from fatal...

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Hlavní autoři:	Yildiz Sengul, MD, Emily Gosche, MD, Todd Hazelton, MD
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Elsevier 2025-09-01
Edice:	Radiology Case Reports
Témata:	Surfactant Protein C SP-C gene mutation Adulthood interstitial lung disease Pulmonary fibrosis CT scan
On-line přístup:	http://www.sciencedirect.com/science/article/pii/S1930043325004844
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