Iridogoniodysgenesis Type 1Symptoms, Doctors, Treatments, Advances & More
Iridogoniodysgenesis Type 1 Overview
Learn About Iridogoniodysgenesis Type 1
Sentara Surgery Specialists
Arthur Vayer is a General Surgeon and a Colorectal Surgeon practicing medicine in Woodbridge, Virginia. Dr. Vayer is rated as an Advanced provider by MediFind in the treatment of Iridogoniodysgenesis Type 1. He is also highly rated in 18 other conditions, according to our data. His clinical expertise encompasses Lymphangiectasis, Primary Intestinal Lymphangiectasia, Meige Disease, Colostomy, and Hernia Surgery. Dr. Vayer is board certified in American Board Of Surgery - Surgery (General Surgery) - 2027. Dr. Vayer is currently accepting new patients.
Paul Chrystal practices practicing medicine in Toronto, Canada. Mr. Chrystal is rated as an Elite expert by MediFind in the treatment of Iridogoniodysgenesis Type 1. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Iridogoniodysgenesis Type 1, Axenfeld-Rieger Syndrome, Aniridia, and Usher Syndrome.
Michael K. Rosenthal D.O. PC
Michael Rosenthal is a General Surgeon practicing medicine in Wilmington, Delaware. Dr. Rosenthal is rated as a Distinguished provider by MediFind in the treatment of Iridogoniodysgenesis Type 1. He is also highly rated in 14 other conditions, according to our data. His clinical expertise encompasses Iridogoniodysgenesis Type 1, Granulomatous Hypophysitis, Lymphomatoid Granulomatosis, and Necrotizing Granuloma. Dr. Rosenthal 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: May 10, 2022
Published By: Genetic and Rare Diseases Informnation Center
