Overview
Anusha Uttarilli practices in Manipala, India. Ms. Uttarilli is rated as an Advanced expert by MediFind in the treatment of X-Linked Spondyloepiphyseal Dysplasia Tarda. Her top areas of expertise are Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), Mongolian Blue Spots, Visceromegaly, and Mucopolysaccharidoses (MPS).
Her clinical research consists of co-authoring 12 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of X-Linked Spondyloepiphyseal Dysplasia Tarda.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts 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.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as 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.
Learn more about MediFind’s expert tiers
- Advanced
- Brachydactyly Mononen TypeMs. Uttarilli isAdvanced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyMs. Uttarilli isAdvanced. Learn about Chondrodystrophy.
- Mongolian Blue SpotsMs. Uttarilli isAdvanced. Learn about Mongolian Blue Spots.
- Mucopolysaccharidoses (MPS)Ms. Uttarilli isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Schwartz-Jampel SyndromeMs. Uttarilli isAdvanced. Learn about Schwartz-Jampel Syndrome.
- Experienced
- GangliosidosisMs. Uttarilli isExperienced. Learn about Gangliosidosis.
- GM1 GangliosidosisMs. Uttarilli isExperienced. Learn about GM1 Gangliosidosis.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)