Closing Gaps in the Recognition & Detection of Niemann-Pick Disease Type C

Guest: Caroline Hastings, MD <br> Guest: Raymond Y. Wang, MD <br> <p>Niemann-Pick disease type C (NPC) is an ultra-rare, inherited, neurodegenerative disease with life-threatening complications. Due to its highly variable onset of neurological symptoms throughout one’s lifespan, recognizing and establishing diagnosis for NPC can be challenging for any clinician.</p> <p>That’s why Drs. Caroline Hastings and Raymond Y. Wang join Dr. Jennifer Caudle to help address those challenges with a detailed look at this genetic condition, the factors underlying its variable onset and course, and strategies to improve recognition, cross-specialty communications, and time to diagnosis. </p> <p style="text-align: right;">Copyright ©2021 Orphazyme A/S. All rights reserved.<br />NP-USA-1492-v1<br />ORPHAZYME is a trademark or registered trademark of Orphazyme A/S.</p>