Overview
Carla Asteggiano practices in Cordoba, Argentina. Ms. Asteggiano is rated as an Advanced expert by MediFind in the treatment of Hereditary Multiple Osteochondromas. Her top areas of expertise are Hereditary Multiple Osteochondromas, Osteochondroma, West Syndrome, and PMM2-Congenital Disorder of Glycosylation.
Her clinical research consists of co-authoring 13 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 5 articles in the study of Hereditary Multiple Osteochondromas.
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
- Hereditary Multiple OsteochondromasMs. Asteggiano isAdvanced. Learn about Hereditary Multiple Osteochondromas.
- OsteochondromaMs. Asteggiano isAdvanced. Learn about Osteochondroma.
- West SyndromeMs. Asteggiano isAdvanced. Learn about West Syndrome.
- Experienced
- Classic GalactosemiaMs. Asteggiano isExperienced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMs. Asteggiano isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Asteggiano isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Asteggiano isExperienced. Learn about Galactosemia.
- HypochondroplasiaMs. Asteggiano isExperienced. Learn about Hypochondroplasia.
- PMM2-Congenital Disorder of GlycosylationMs. Asteggiano isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.