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Delayed diagnosis of a patient with Usher syndrome 1C in a Louisiana Acadian family highlights the necessity of timely genetic testing for the diagnosis and management of congenital hearing loss
Umrigar, Ayesha, Musso, Amanda, Mercer, Danielle, Hurley, Annette, Glausier, Cassondra, Bakeer, Mona, Marble, Michael, Hicks, Chindo, Tsien, FernVolume:
5
Language:
english
Journal:
SAGE Open Medical Case Reports
DOI:
10.1177/2050313X17745904
Date:
December, 2017
File:
PDF, 122 KB
english, 2017