Overview
Pankaj Prasun is a Medical Genetics specialist and a Pediatrics provider in Madison, Wisconsin. Dr. Prasun and is rated as an Experienced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Methylmalonic Acidemia with Homocystinuria, Ornithine Transcarbamylase Deficiency, Homocystinuria, and Ornithine Translocase Deficiency. Dr. Prasun is currently accepting new patients.
His clinical research consists of co-authoring 31 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- UnitedHealthcare
- Humana
Locations
600 Highland Ave, Madison, WI 53792
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
University Of Wisconsin Medical Foundation Inc
William Rhead is a Medical Genetics specialist and a Pediatrics provider in Madison, Wisconsin. Dr. Rhead and is rated as a Distinguished provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Urea Cycle Disorders (UCD), Gaucher Disease Type 1, Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Rhead is currently accepting new patients.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Advanced
- Homocystinuria
- Inborn Amino Acid Metabolism Disorder
- Methylmalonic Acidemia with Homocystinuria
- Ornithine Transcarbamylase Deficiency
- Ornithine Translocase Deficiency
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Arginase Deficiency
- Argininosuccinic Aciduria
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Cockayne Syndrome
- Cockayne Syndrome Type 1