Dextrocardia with Situs InversusSymptoms, Doctors, Treatments, Advances & More
Dextrocardia with Situs Inversus Overview
Learn About Dextrocardia with Situs Inversus
- Dextrocardia with situs inversus
- Situs inversus totalis
Sharon Dell practices in Vancouver, Canada. Dell is rated as an Elite expert by MediFind in the treatment of Dextrocardia with Situs Inversus. Their top areas of expertise are Ciliary Dyskinesia-Bronchiectasis, Drug Induced Dyskinesia, Dextrocardia with Situs Inversus, and Dextrocardia.
Atrium Health Levine Children's HEARTest Yard Congenital Heart Center
Jorge Alegria is a Cardiologist in Charlotte, North Carolina. Dr. Alegria is rated as an Advanced provider by MediFind in the treatment of Dextrocardia with Situs Inversus. His top areas of expertise are Transposition of the Great Arteries, Tetralogy of Fallot, Dextrocardia with Situs Inversus, and Situs Inversus. Dr. Alegria is currently accepting new patients.
Heymut Omran practices in Muenster, Germany. Omran is rated as an Elite expert by MediFind in the treatment of Dextrocardia with Situs Inversus. Their top areas of expertise are Situs Inversus, Ciliary Dyskinesia-Bronchiectasis, Kartagener Syndrome, and Drug Induced Dyskinesia.
Summary: Primary Ciliary Dyskinesias (PCD) are rare, autosomal recessive respiratory diseases, due to a defect in mucociliary clearance linked to abnormalities in the structure and/or function of the cilia. The variety of ciliary abnormalities identified reflects the genetic heterogeneity of PCDs. The thirty or so genes currently implicated explain the pathology in about half of the patients. PCDs are char...
Summary: The Ear-Nose-Throat (ENT) Prospective International Cohort of patients with Primary Ciliary Dyskinesia (EPIC-PCD) is a prospective observational clinical cohort study, set up as a multinational multi-centre study. It is embedded into routine patient care of participating reference centres for PCD and patients keep being managed according to local procedures and guidelines.
Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center

