VUMC team discovers new genetic disease

Researchers at Vanderbilt University Medical Center have discovered a new genetic disease that causes a severe form of neurogenic orthostatic hypotension, a rapid drop in blood pressure upon standing that can cause fainting.

Undiagnosed Diseases Network helps guide girl’s medical journey

On July 6, 2017, the Krauter family of Hiawatha, Kansas, received a belated 4th birthday present for their younger daughter, Mady — a diagnosis for a host of worsening neurological symptoms that they first noticed when she was 3 months old.

VUMC’s Undiagnosed Diseases Network site gains NIH renewal

UDN program dedicated to solving medical mysteries

It’s human nature to need answers. Patients with debilitating symptoms need a diagnosis — somewhere to place the blame, a starting point to search for answers.

Hamid named to lead Division of Pediatric Genetics

Rizwan Hamid, M.D., Ph.D., associate professor of Pediatrics at Vanderbilt University, has been named chief of the Division of Pediatric Genetics and Genomic Medicine, effective Jan. 1, 2017.

Vanderbilt is one of seven centers now accepting patients for Undiagnosed Diseases Network

Eighteen-year-old Rachel Barnett of Robertson County is one of the first patients to be enrolled in the Undiagnosed Diseases Network (UDN) at Vanderbilt University Medical Center — one of seven medical centers around the country participating in a clinical research initiative of the National Institutes of Health to identify rare disorders in patients.