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Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment

期刊

WORLD JOURNAL OF PEDIATRICS
卷 13, 期 3, 页码 197-201

出版社

ZHEJIANG UNIV SCH MEDICINE
DOI: 10.1007/s12519-017-0036-3

关键词

Duchene muscular dystrophy; neurology; neuromuscular disorders; newborn screening

资金

  1. Muscular Dystrophy Association
  2. Sarepta
  3. Marathon
  4. PerkinElmer
  5. National High Technology Research and Development Program (863 Program) [2015AA020513]
  6. Zhejiang Provincial Natural Science Foundation of China [LY16H0900007]

向作者/读者索取更多资源

Background: Newborn screening for Duchenne muscular dystrophy (DMD) is currently being initiated in Zhejiang Province, China and is under consideration in other countries, including the United States. As China begins to implement DMD newborn screening (DMD-NBS), there is ongoing discussion regarding the steps forward for follow up care of positively identified patients as well as false positive and false negative results. Data sources: Relevant papers related to DMD-NBS, and NBS in China were reviewed in PubMed. Results: The current state of DMD-NBS is discussed, along with the steps needed to effectively screen infants for this disease in China, recommendations for establishment of follow up care in patients with positive and negative screens, and measurement of patient outcomes. Conclusions: Zhejiang Province, China is ready to implement DMD-NBS. Future challenges that exist for this program, and other countries, include the ability to track patients, assist with access to care, and ensure adequate follow-up care according to evidence-based guidelines. In addition, China's large rural population, lack of specialty providers, and difficulty in educating patients regarding the benefits of treatment create challenges that will need to be addressed.

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