Suzanne Hart, Ph.D.
Medical Genetics Branch
Medical Genetics and Genomic Medicine Training Program
A.A. Diablo Valley College, 1983
B.S. California State University, 1985
Ph.D. Virginia Commonwealth University, 1990
10 CENTER DR, MSC 1253
BETHESDA, MD 20892-1253
Dr. Hart uses molecular and biochemical techniques to understand genetic diseases of the teeth, oral cavity and kidney.
Gum tissue is important in tooth development, with gum health contributing to overall well-being, appearance and the ability to eat and speak properly. Gum overgrowth can occur as an isolated inherited condition, as part of a genetic syndrome, or as a side effect of certain medications. Dr. Hart and colleagues discovered the only gene, SOS1, known to be involved in isolated hereditary gingival fibromatosis, a rare autosomal dominant form of gum overgrowth. She is also studying syndromic forms of gum overgrowth, such as Zimmerman-Laband syndrome and juvenile hyaline fibromatosis, as well as gum overgrowth attributed to various medications.
Dr. Hart also investigates disorders that affect the enamel or dentin inside teeth. Dr. Hart's group has discovered mutations in a number of genes (e.g., AMELX, ENAM, KLK4, MMP20, and DSPP). A large collection of samples compiled by her group since 1991 are routinely re-examined as new technologies become available, enabling the identification of additional genes involved in the development of tooth defects.
Dr. Hart's group identified the CTCS gene defect in Papillon-Lefevre syndrome, an autosomal recessive disorder characterized by keratosis of the palms and soles of the feet, as well as pronounced periodontal disease. Children with this condition suffer mouth inflammation and problems with their newly erupted teeth. Primary teeth are typically lost by age 4, with loss of permanent teeth by age 20.
Dr. Hart also studies medullary cystic kidney disease (MCKD), an inherited disorder associated with gradual loss of kidney function. Dr. Hart and colleagues identified MUC1 and UMOD as the causative genes in MCKD types 1 and 2, respectively. They have also identified REN mutations as the cause of one form of anemia and chronic kidney failure. Understanding the genetic causes of various forms of kidney disease may lead to new therapies.
Suzanne Hart received her B.S. in biology from California State University, Hayward (now called East Bay University) in 1985. She earned her Ph.D. in Human Genetics from the Medical College of Virginia (now called Virginia Commonwealth University) in 1990. Her doctoral thesis was "Biochemical and Immunological Characterization of Serum Biotinidase in Normal and Biotinidase-deficient States." She is an ABMG board-certified clinical biochemical and medical geneticist. She completed her postdoctoral training with Larry Tabak, D.D.S., Ph.D., at the University of Rochester.
Her first faculty position was at Eastman Dental Center. Subsequently she joined Wake Forest University as an assistant professor, where she directed three of the diagnostic laboratories: Maternal Serum Screening, Biochemical Genetics and Molecular Genetics. While at Wake Forest, she established a multidisciplinary clinic for Prader-Willi syndrome. She then joined the faculty at the University of Pittsburgh as an associate professor where she was the director of the Genetics and Proteomics Core Facilities. She joined NHGRI in 2003.
She is currently an associate investigator and deputy director of the Medical Genetics and Genomic Medicine Fellowship Training Program. Dr. Hart is the coordinator or co-coordinator of four graduate level courses offered through the Foundation for Advanced Education in the Sciences office. She uses molecular and biochemical techniques to understand genetic diseases of the teeth, the oral cavity and the kidney.
Last Updated: January 6, 2015