Interstitial Lung Disease in Adulthood Associated with Surfactant Protein C Gene Mutation in a Patient with a History of Lipoid Pneumonia in Infancy
Author:
Affiliation:
1. Department of Respiratory Medicine, Kumamoto University Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/62/17/62_0980-22/_pdf
Reference17 articles.
1. 1. Wert SE, Whitsett JA, Nogee LM. Genetic disorders of surfactant dysfunction. Pediatr Dev Pathol 12: 253-274, 2009.
2. 2. Akimoto T, Cho K, Hayasaka I, et al. Hereditary interstitial lung diseases manifesting in early childhood in Japan. Pediatr Res 76: 453-458, 2014.
3. 3. van Moorsel CH, van Oosterhout MF, Barlo NP, et al. Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort. Am J Respir Crit Care Med 182: 1419-1425, 2010.
4. 4. Kröner C, Reu S, Teusch V, et al. Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients. Eur Respir J 46: 197-206, 2015.
5. 5. Litao MK, Hayes D Jr., Chiwane S, Nogee LM, Kurland G, Guglani L. A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy. Pediatr Pulmonol 52: 57-68, 2017.
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