Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5953704 | Chest | 2015 | 8 Pages |
Abstract
This report identifies HPS as a frequent cause of dyspnea in telomerase and telomere gene mutation carriers. While it usually precedes the development of parenchymal lung disease, HPS may also co-occur with pulmonary fibrosis and emphysema. Recognizing this genetic diagnosis is critical for management, especially in the lung and liver transplantation setting.
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Authors
Amany I. MD, Naudia L. MD, Susan E. BS, Ayman MD, Amy E. MD, Jolan E. MD, PhD, Sabrina C. MD, James P. MD, Julie MD, PhD, Allen R. MD, Robert A. MD, PhD, Ihab R. MD, Mary MD,