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Multiple Malformation clinical trials

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NCT ID: NCT02551081 Recruiting - Genetic Disease Clinical Trials

Genomic Sequencing and Personalized Treatment for Birth Defects in Neonatal Intensive Care Units

Start date: October 1, 2015
Phase:
Study type: Observational

The purpose of study is to evaluate the benefits of using the Next Generation Sequencing Technology to diagnose birth defects and genetic diseases. The results from genomic sequencing can also significantly shorten the time of examination, improve the diagnosis rate, guide the clinical treatments. So the ultimate goal is individualized or personalized therapy and promote prognosis.