Related Experiment Video For Hypothyroidism
Updated: Mar 1, 2026
08:58
Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs
Published on: October 31, 2025
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Interstitial lung disease of infancy caused by a new NKX2-1 mutation
Khalid H Safi1, John A Bernat1, Catherine E Keegan1
1Department of Pediatrics and Communicable Diseases University of Michigan Medical School Ann Arbor Michigan USA.
Clinical Case Reports
|June 8, 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.
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