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Isolated pulmonary interstitial glycogenosis associated with alveolar growth abnormalities: A long-term follow-up study.

Olaia SardónAlba Torrent VernettaSandra Rovira-AmigoMegan K DishopJoan Carles FerreresAlexandra NavarroPaula CorcueraJavier Korta-MuruaPilar García PeñaElena Pérez-BelmonteAna VillaresNúria CamatsMónica Fernández-CancioAntonio CarrascosaEduardo G Pérez-YarzaAntonio Moreno-Galdó
Published in: Pediatric pulmonology (2019)
Although the patients with PIG in the absence of other associated pathologies had a good clinical outcome, significant radiographic alterations and sequelae in lung function were still observed after a median follow-up of 12 years, suggesting that PIG is a marker of some other persistent abnormalities in lung growth, which have effects beyond the symptomatic period.
Keyphrases
  • lung function
  • cystic fibrosis
  • chronic obstructive pulmonary disease
  • air pollution
  • pulmonary hypertension