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Editorial

. 2020 Mar 17;4(1):59-60.

doi: 10.1002/ped4.12179. eCollection 2020 Mar.

Genetic testing for rare pediatric lung disorders: The promise and the pitfalls

Lawrence M Nogee¹

Affiliations

PMID: 32851344
PMCID: PMC7331405
DOI: 10.1002/ped4.12179

Editorial

Genetic testing for rare pediatric lung disorders: The promise and the pitfalls

Lawrence M Nogee. Pediatr Investig. 2020.

. 2020 Mar 17;4(1):59-60.

doi: 10.1002/ped4.12179. eCollection 2020 Mar.

Author

Lawrence M Nogee¹

Affiliation

¹ Eudowood Division of Neonatology Department of Pediatrics Johns Hopkins University School of Medicine Baltimore Maryland USA.

PMID: 32851344
PMCID: PMC7331405
DOI: 10.1002/ped4.12179

No abstract available

PubMed Disclaimer

Conflict of interest statement

None.

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References

1. Nogee LM. Genetic causes of surfactant protein abnormalities. Curr Opin Pediatr. 2019;31:330–339. - PMC - PubMed
1. Tang X, Shen Y, Zhou C, Yang H, Liu H, Li H, et al. Surfactant protein C dysfunction with new clinical insights for diffuse alveolar hemorrhage and autoimmunity. Pediatr Invest. 2019;3:201–206. - PMC - PubMed
1. Cameron HS, Somaschini M, Carrera P, Hamvas A, Whitsett JA, Wert SE, et al. A common mutation in the surfactant protein C gene associated with lung disease. J Pediatr. 2005;146:370–375. - PubMed
1. Kroner C, Reu S, Teusch V, Schams A, Grimmelt AC, Barker M, et al. Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients. Eur Respir J. 2015;46:197–206. - PubMed
1. Stevens PA, Pettenazzo A, Brasch F, Mulugeta S, Baritussio A, Ochs M, et al. Nonspecific interstitial pneumonia, alveolar proteinosis, and abnormal proprotein trafficking resulting from a spontaneous mutation in the surfactant protein C gene. Pediatr Res. 2005;57:89–98. - PubMed

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