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- Title
Interstitial lung disease of infancy caused by a new NKX2-1 mutation.
- Authors
Safi, Khalid H.; Bernat, John A.; Keegan, Catherine E; Ahmad, Ayesha; Hershenson, Marc B.; Arteta, Manuel
- Abstract
Key Clinical Message 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 .
- Subjects
INTERSTITIAL lung diseases in children; GENETIC mutation; GENEALOGY; NEUROLOGY; DIAGNOSIS
- Publication
Clinical Case Reports, 2017, Vol 5, Issue 6, p739
- ISSN
2050-0904
- Publication type
Article
- DOI
10.1002/ccr3.901