Overview
Udhaya Kotecha practices practicing medicine in Ahmedabad, India.
Kotecha is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Simpson-Golabi-Behmel Syndrome, Fructose-1,6-Bisphosphatase Deficiency, Congenital Contractures, and Arthrogryposis Multiplex Congenita.
They are actively involved in clinical research, co-authoring 24 peer reviewed articles.
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.
Frequently Asked Questions about Udhaya H. Kotecha
Is Udhaya H. Kotecha a top-rated expert for Simpson-Golabi-Behmel Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Udhaya H. Kotecha is classified as an Advanced expert for Simpson-Golabi-Behmel Syndrome, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Udhaya H. Kotecha participate in research or clinical trials?
Yes. Udhaya H. Kotecha has published 24 articles and abstracts on conditions like Simpson-Golabi-Behmel Syndrome. You can view a list of Udhaya H. Kotecha's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Simpson-Golabi-Behmel Syndrome
- Experienced
- Arthrogryposis Multiplex Congenita
- Autoimmune Hemolytic AnemiaKotecha isExperienced. Learn about Autoimmune Hemolytic Anemia.
- Autosomal Dominant Hyper IgE Syndrome
- Cold UrticariaKotecha isExperienced. Learn about Cold Urticaria.
- Congenital ContracturesKotecha isExperienced. Learn about Congenital Contractures.
- Familial Cold Autoinflammatory Syndrome
- Fructose-1,6-Bisphosphatase Deficiency
- GigantismKotecha isExperienced. Learn about Gigantism.
- Griscelli SyndromeKotecha isExperienced. Learn about Griscelli Syndrome.
- Hyper IgE SyndromeKotecha isExperienced. Learn about Hyper IgE Syndrome.
- Metabolic AcidosisKotecha isExperienced. Learn about Metabolic Acidosis.
- Muckle-Wells SyndromeKotecha isExperienced. Learn about Muckle-Wells Syndrome.
- Neonatal Onset Multisystem Inflammatory Disease
- Spinocerebellar Ataxia Type 3Kotecha isExperienced. Learn about Spinocerebellar Ataxia Type 3.
- Striatonigral Degeneration Infantile