Rare genetic interstitial lung diseases: a pictorial essay
The main monogenic causes of pulmonary fibrosis in adults are mutations in telomere-related genes. These mutations may be associated with extrapulmonary signs (hepatic, haematological and dermatological) and typically present radiologically as usual interstitial pneumonia or unclassifiable fibrosis....
Saved in:
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
European Respiratory Society
2024-11-01
|
Series: | European Respiratory Review |
Online Access: | http://err.ersjournals.com/content/33/174/240101.full |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|