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Retinal Whitening After Lung Transplant for Cystic Fibrosis

Christopher D Conrady1, Hakan Demirci1, Thomas J Wubben1

  • 1Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor.

JAMA Ophthalmology
|July 10, 2020
PubMed
Abstract

No abstract available in PubMed .

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Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
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