Newborn screening for Duchenne muscular dystrophy: A two‐year pilot study
Abstract Objective Duchenne muscular dystrophy (DMD) is an X‐linked disorder resulting in progressive muscle weakness and atrophy, cardiomyopathy, and in late stages, cardiorespiratory impairment, and death. As treatments for DMD have expanded, a DMD newborn screening (NBS) pilot study was conducted...
Main Authors: | Norma P. Tavakoli, Dorota Gruber, Niki Armstrong, Wendy K. Chung, Breanne Maloney, Sunju Park, Julia Wynn, Carrie Koval‐Burt, Lorraine Verdade, David H. Tegay, Lilian L. Cohen, Natasha Shapiro, Annie Kennedy, Garey Noritz, Emma Ciafaloni, Barry Weinberger, Marty Ellington Jr, Charles Schleien, Regina Spinazzola, Sunil Sood, Amy Brower, Michele Lloyd‐Puryear, Michele Caggana, the Duchenne Muscular Dystrophy Pilot Study Group |
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Format: | Article |
Language: | English |
Published: |
Wiley
2023-08-01
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Series: | Annals of Clinical and Translational Neurology |
Online Access: | https://doi.org/10.1002/acn3.51829 |
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