Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Oct;58(10):2719-2724.
doi: 10.1002/ppul.26603. Epub 2023 Jul 26.

Pediatric Pulmonology 2022 year in review: Rare and diffuse lung disease

Andrew T Barber  1 , Deborah R Liptzin  2   3   4 , William A Gower  5 , Daniel M Hinds  6
Affiliations
Review

Pediatric Pulmonology 2022 year in review: Rare and diffuse lung disease

Andrew T Barber et al. Pediatr Pulmonol. 2023 Oct.

Abstract

The field of rare and diffuse pediatric lung disease continues to evolve and expand rapidly as clinicians and researchers make advancements in the diagnosis and treatment of children's interstitial and diffuse lung disease, non-cystic fibrosis bronchiectasis, and primary ciliary dyskinesia. Papers published on these topics in Pediatric Pulmonology and other journals in 2022 describe newly recognized disorders, elucidate disease mechanisms and courses, explore potential biomarkers, and assess novel treatments. In this review, we will discuss these important advancements and place them in the context of existing literature.

Keywords: bronchiectasis; congenital abnormalities; interstitial lung disease; primary ciliary dyskinesia.

PubMed Disclaimer

References

REFERENCES

    1. Bradford L, Ross MK, Minso J, et al. Interstitial lung disease in children with rubinstein-taybi syndrome. Pediatr Pulmonol. 2022;57(1):264-272.
    1. Shulenin S, Nogee LM, Annilo T, Wert SE, Whitsett JA, Dean M. Abca3 gene mutations in newborns with fatal surfactant deficiency. N Engl J Med. 2004;350(13):1296-1303.
    1. Wambach JA, Casey AM, Fishman MP, et al. Genotype-phenotype correlations for infants and children with abca3 deficiency. Am J Respir Crit Care Med. 2014;189(12):1538-1543.
    1. Xu KK, Wegner DJ, Geurts LC, et al. Biologic characterization of abca3 variants in lung tissue from infants and children with abca3 deficiency. Pediatr Pulmonol. 2022;57(5):1325-1330.
    1. Liptzin DR, Pickett K, Brinton JT, et al. Neuroendocrine cell hyperplasia of infancy. clinical score and comorbidities. Ann Am Thorac Soc. 2020;17(6):724-728.

LinkOut - more resources