Persistent Lung Disease in Adults with NKX2.1 Mutation and Familial Neuroendocrine Cell Hyperplasia of Infancy

Rationale: Neuroendocrine cell hyperplasia of infancy (NEHI) is a diffuse lung disease that presents in infancy and improves during childhood. Long-term outcomes have not previously been described. In one familial cohort, we have reported that NEHI is associated with a heterozygous variant of NKX2.1...

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Foilsithe in:Ann Am Thorac Soc
Main Authors: Nevel, Rebekah J., Garnett, Errine T., Worrell, John A., Morton, Ronald L., Nogee, Lawrence M., Blackwell, Timothy S., Young, Lisa R.
Formáid: Artigo
Teanga:Inglês
Foilsithe: American Thoracic Society 2016
Ábhair:
Original Research
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5021081/
https://ncbi.nlm.nih.gov/pubmed/27187870
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/AnnalsATS.201603-155BC
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