The Smith Family Clinic for Genomic Medicine, LLC., a wholly-owned subsidiary of HudsonAlpha Institute for Biotechnology, has been established to diagnose patients with undiagnosed and misdiagnosed diseases. Patients will be seen by a clinical geneticist who will evaluate symptoms, or patient phenotype, and determine whether whole genome sequencing or another genetic test is appropriate. The data found from the genomic sequence is then interpreted clinically to identify variants, or changes in the DNA, linked to the disease. Get in touch 256-327-9640 and visit https://smithfamilyclinic.org/.
Confusion, nausea, fever, anger, then back to normal: this was Lauren Vandiver’s life beginning in early childhood. Her parents, Phillip and Angela Vandiver, spent more than twenty years asking the…
Rare disease patients spend an average of eight years searching for a diagnosis, and for some, that search can last decades. April Hudson of Quinton, Ala., began showing symptoms of…
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