Zarko's Story: Genomic Medicine In Action
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- Опубліковано 12 кві 2018
- Zarko Stanacev experienced years of mysterious debilitating symptoms. He applied to NIH's Undiagnosed Diseases Network (UDN) and had his genome was sequenced and interpreted by a team including Dr. William Gahl at the U.S. National Institutes of Health. They found a mutation in the gene NLRP3, which causes abnormal inflammation throughout the body. After only one treatment with a medicine to dampen this inflammation, Zarko's symptoms improved.
Video was produced by 42 Degrees North Media for the National Human Genome Research Institute.