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Rapid Genetic Diagnosis Employing Next Generation Sequencing for Critical Illness in Infants and Children

Acute Disease Clinical Trial

Official title:
Rapid Genetic Diagnosis Employing Next Generation Sequencing for Critical Illness in Infants and Children

Clinical Trial Summary

Under the joint efforts of genetic and intensive expert, to establish the high-throughput whole exon sequencing(WES) and analysis all the possible pathogenic genes. To provide patient with the appropriate treatment for genetic disease. Besides, it can identify the genetic factor of idiosyncrasy or susceptibility to explain the medical difficulties and give patients personalized advice.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03175692
Study type Observational
Source National Taiwan University Hospital
Contact
Status Enrolling by invitation
Phase N/A
Start date June 14, 2017
Completion date May 2020
View Details
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