Hyperlipidemia
Miniature Schnauzers are commonly affected by idiopathic familial hyperlipidemia. This means that many members of the breed have high blood lipid levels (triglycerides and sometimes cholesterol) without a known underlying cause. This is also referred to as primary hyperlipidemia. We are investigating a mutation that may increase the risk for moderate to severe hyperlipidemia in Miniature Schnauzers. If you would like to find out more about this study or submit a DNA sample from a Schnauzer with idiopathic/primary hyperlipidemia, please contact Dr. Furrow at 612-625-7493 or [email protected].
Funding
About the investigator
Dr. Furrow is a Small Animal Internist and Assistant Professor at the University of Minnesota College of Veterinary Medicine. She first became interested in the genetic basis of canine diseases when she was an undergraduate at Harvard University. She was offered a summer position in the Section of Medical Genetics at the University of Pennsylvania. One of her roles that summer included assistance in a study on the genetic muscular disease myotonia congenita in Miniature Schnauzers. Dr. Furrow later attended the University of Pennsylvania Veterinary School where a NIH-Merck grant enabled her to continue research on genetic diseases. Dr. Furrow completed her Internal Medicine residency and PhD at the University of Minnesota and is currently a member of the Canine and Equine Genetics Laboratory. Dr. Furrow's ultimate goal is to find better ways to prevent and treat genetic diseases. She also has a personal attachment to one of the high-risk breeds, as her parents-in-law have always had Miniature Schnauzers.
If you have further questions about this study, please contact Dr. Eva Furrow: 612-625-7493 or [email protected].
Contact Us
Canine Genetics Lab
University of Minnesota
1988 Fitch Ave
AS/VM 295
St. Paul, MN 55108
[email protected]
612.624.5322
z.umn.edu/caninegenetics
Canine Genetic Testing
- 2,8- Dihydroxyadenine Urinary Stones
- Alaskan Malamute Polyneuropathy
- Exercise Induced Collapse
- Hereditary Calcium Oxalate Urolithiasis, Type 1
- Inflammatory Myopathy (Myositis)
- Leonberger Health Panel
- Leukoencephalomyelopathy
- Neuronal Degeneration
- Persistent Müllerian Duct Syndrome
- Saint Bernard Laryngeal Paralysis & Polyneuropathy
- Sarcoglycan Deficient Muscular Dystrophy
- Toy Manchester Terrier / English Toy Terrier Health Panel
- Ullrich Congenital Muscular Dystrophy
- Xanthinuria
Canine Genetic Research
- Addison's Disease - Autoantibody Study
- Addison's Disease - Genetics Study
- Addison's Disease - MHC Study
- Atypical Seizures / Paroxysmal Dyskinesia
- Border Collie Collapse
- Calcium Oxalate Urinary Stones
- Hyperlipidemia
- Idiopathic Epilepsy
- Immune-Mediated Hemolytic Anemia (IMHA)
- Leonberger Polyneuropathy / Laryngeal Paralysis
- Pulmonary Fibrosis
- Whippet Exercise Induced Hyperthermia