Learn About Hypolipoproteinemia
- Hypolipoproteinemia
Penn Heart And Vascular Center
Daniel Rader is a primary care provider, a Cardiologist and a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Rader is rated as an Elite provider by MediFind in the treatment of Hypolipoproteinemia. His top areas of expertise are High Cholesterol, Familial Hypercholesterolemia, Homozygous Familial Hypercholesterolemia (HoFH), Coronary Heart Disease, and Heart Transplant. Dr. Rader is currently accepting new patients.
Texas Health Family Care
Richard Townsend is a primary care provider, practicing in General Practice in Richardson, Texas. Dr. Townsend is rated as an Advanced provider by MediFind in the treatment of Hypolipoproteinemia. His top areas of expertise are Vitamin D Deficiency, Gilbert Syndrome, High Cholesterol, and Nephrosclerosis.
Texas Health Family Care
Karna Gocke is a primary care provider, practicing in Family Medicine in Prosper, Texas. Dr. Gocke is rated as an Advanced provider by MediFind in the treatment of Hypolipoproteinemia. Her top areas of expertise are Vitamin D Deficiency, Peripheral Neuropathy, Familial Hypertriglyceridemia, Obesity, and Intrauterine Device Insertion.
Summary: The purpose of the LCAT (Lecithin cholesterol acyl transferase) Natural History Study (LCAT NHS) is to help identify people with a mutation in a gene called LCAT, collect and store information about their medical history and disease course, and to assess for associations and follow changes in clinical features and biomarkers of disease. This information will help health care providers better under...
Summary: The My Retina Tracker® Registry is sponsored by the Foundation Fighting Blindness and is for people affected by one of the rare inherited retinal degenerative diseases studied by the Foundation. It is a patient-initiated registry accessible via a secure on-line portal at www.MyRetinaTracker.org. Affected individuals who register are guided to create a profile that captures their perspective on the...
Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center