Overview
Kwok Tsang practices practicing medicine in Lika, China.
Mr. Tsang is highly rated in 2 conditions, according to our data. His clinical expertise encompasses Craniodiaphyseal Dysplasia, Holocarboxylase Synthetase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Achondrogenesis.
He is actively involved in clinical research, co-authoring 10 peer reviewed articles.
Gender
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 Kwok Y. Tsang
Is Kwok Y. Tsang a top-rated expert for Craniodiaphyseal Dysplasia?
MediFind is an objective health platform that identifies experts based on real-world data. Kwok Y. Tsang is classified as an Advanced expert for Craniodiaphyseal Dysplasia, 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 Kwok Y. Tsang participate in research or clinical trials?
Yes. Kwok Y. Tsang has published 10 articles and abstracts on conditions like Craniodiaphyseal Dysplasia. You can view a list of Kwok Y. Tsang'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
- Craniodiaphyseal DysplasiaMr. Tsang isAdvanced. Learn about Craniodiaphyseal Dysplasia.
- Holocarboxylase Synthetase Deficiency
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- AchondrogenesisMr. Tsang isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaMr. Tsang isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Brachydactyly Mononen TypeMr. Tsang isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyMr. Tsang isExperienced. Learn about Chondrodystrophy.
- CitrullinemiaMr. Tsang isExperienced. Learn about Citrullinemia.
- Glutaric Acidemia Type 2Mr. Tsang isExperienced. Learn about Glutaric Acidemia Type 2.
- Inborn Amino Acid Metabolism DisorderMr. Tsang isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Multiple Carboxylase DeficiencyMr. Tsang isExperienced. Learn about Multiple Carboxylase Deficiency.
- Schwartz-Jampel SyndromeMr. Tsang isExperienced. Learn about Schwartz-Jampel Syndrome.
- Urea Cycle Disorders (UCD)Mr. Tsang isExperienced. Learn about Urea Cycle Disorders (UCD).
- X-Linked Spondyloepiphyseal Dysplasia Tarda