Division of Otolaryngology (Ear, Nose and Throat) Event Listing

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What's New in PCD Research, Diagnosis and Treatment

Boy climbing on outdoor playground

PCD is a rare, genetically heterogeneous, autosomal recessive disorder leading to impaired ciliary clearance from the lower airways, middle ear, and paranasal sinuses. This webinar will Identify the classic pediatric phenotype in PCD and recognize the current diagnostic tools and their limitations.

Date:
Oct 12, 2021 from 8 a.m. - 9 a.m. (ET)