Arthrogryposis Multiplex Congenita Overview
Learn About Arthrogryposis Multiplex Congenita
- Arthrogryposis multiplex congenita
- Arthrogryposis
- Congenital arthromyodysplasia
- Congenital multiple arthrogryposis
- Fibrous ankylosis of multiple joints
- Guerin-Stern syndrome
- Guérin-Stern syndrome
- Myodystrophia fetalis deformans
- Otto syndrome
- Rocher-Sheldon syndrome
- Rossi syndrome
Shriners Hospital For Children
Harold Van Bosse-Vanbosse is a Pediatric Orthopedics specialist and an Orthopedics provider in Philadelphia, PA. Dr. Van Bosse-Vanbosse and is rated as an Elite provider by MediFind in the treatment of Arthrogryposis Multiplex Congenita. His top areas of expertise are Congenital Contractures, Arthrogryposis Multiplex Congenita, Clubfoot, Osteotomy, and Hip Replacement. Dr. Van Bosse-Vanbosse is currently accepting new patients.
Noemi Oliel-Dahan practices in Montreal, Canada. Ms. Oliel-Dahan and is rated as an Elite expert by MediFind in the treatment of Arthrogryposis Multiplex Congenita. Her top areas of expertise are Congenital Contractures, Arthrogryposis Multiplex Congenita, Cerebral Palsy, Multiple Pterygium Syndrome, and Osteotomy.
Klaus Dieterich practices in Grenoble, France. Mr. Dieterich and is rated as an Elite expert by MediFind in the treatment of Arthrogryposis Multiplex Congenita. His top areas of expertise are Congenital Contractures, Arthrogryposis Multiplex Congenita, Distal Arthrogryposis, and Distal Arthrogryposis Type 6.
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...
Summary: The purpose of this study is to characterize oxidative stress and the Nrf2 antioxidant response in early stages of Autosomal Dominant Polycystic Kidney Disease (ADPKD), while identifying candidate biomarkers.
Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center