Learn About Frasier Syndrome
Frasier syndrome is a condition that affects the kidneys and genitalia.
Mutations in the WT1 gene cause Frasier syndrome. The WT1 gene provides instructions for making a protein that regulates the activity of other genes by attaching (binding) to specific regions of DNA. On the basis of this action, the WT1 protein is called a transcription factor. The WT1 protein plays a role in the development of the kidneys and gonads (ovaries in females and testes in males) before birth.
Frasier syndrome is thought to be a rare condition; approximately 50 cases have been described in the scientific literature.
This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.
Emergency And Acute Care Medical Corporation
Guy Lund is a Nephrologist in San Diego, California. Dr. Lund and is rated as a Distinguished provider by MediFind in the treatment of Frasier Syndrome. His top areas of expertise are Poststreptococcal Glomerulonephritis, Autosomal Dominant Polycystic Kidney Disease, Polycystic Kidney Disease, and Frasier Syndrome.
Cooper Nephrology PC
Ron Zanger is a Nephrologist in Camden, New Jersey. Dr. Zanger and is rated as a Distinguished provider by MediFind in the treatment of Frasier Syndrome. His top areas of expertise are End-Stage Renal Disease (ESRD), Renovascular Hypertension, Acute Kidney Failure, and Frasier Syndrome. Dr. Zanger is currently accepting new patients.
Cleveland Clinic
Jerin Mathew is a Nephrologist in Cleveland, Ohio. Dr. Mathew and is rated as an Experienced provider by MediFind in the treatment of Frasier Syndrome. His top areas of expertise are Acute Kidney Failure, End-Stage Renal Disease (ESRD), Chronic Kidney Disease, and High Potassium Level. Dr. Mathew is currently accepting new patients.
Summary: CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, in...
Published Date: March 01, 2013
Published By: National Institutes of Health