Back to Search
Start Over
Interstitial lung disease of infancy caused by a new NKX2-1 mutation.
- Source :
-
Clinical case reports [Clin Case Rep] 2017 Apr 04; Vol. 5 (6), pp. 739-743. Date of Electronic Publication: 2017 Apr 04 (Print Publication: 2017). - Publication Year :
- 2017
-
Abstract
- Patients with personal or family history of congenital hypothyroidism, and/or neurological findings that also have chronic respiratory symptoms may have a mutation in the NKX2.1 gene as the unifying cause of their disease. Brain-lung-thyroid disease is the ensuing condition, which although rare, needs to be part of the differential diagnosis .
Details
- Language :
- English
- ISSN :
- 2050-0904
- Volume :
- 5
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Clinical case reports
- Publication Type :
- Report
- Accession number :
- 28588801
- Full Text :
- https://doi.org/10.1002/ccr3.901