Overview
Zongfu Cao practices practicing medicine in Beijing, China.
Cao is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Joubert Syndrome, Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), and Hermansky-Pudlak Syndrome.
They are actively involved in clinical research, co-authoring 48 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 Zongfu X. Cao
Is Zongfu X. Cao a top-rated expert for Joubert Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Zongfu X. Cao is classified as an Distinguished expert for Joubert 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 Zongfu X. Cao participate in research or clinical trials?
Yes. Zongfu X. Cao has published 48 articles and abstracts on conditions like Joubert Syndrome. You can view a list of Zongfu X. Cao'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
- Distinguished
- Joubert SyndromeCao isDistinguished. Learn about Joubert Syndrome.
- Advanced
- Maternal Hyperphenylalaninemia
- Phenylketonuria (PKU)
- Experienced
- Acrofacial Dysostosis Rodriguez Type
- Acrofrontofacionasal Dysostosis Syndrome
- AlbinismCao isExperienced. Learn about Albinism.
- Blood ClotsCao isExperienced. Learn about Blood Clots.
- CataractCao isExperienced. Learn about Cataract.
- Cone-Rod DystrophyCao isExperienced. Learn about Cone-Rod Dystrophy.
- Congenital CataractCao isExperienced. Learn about Congenital Cataract.
- Crouzon SyndromeCao isExperienced. Learn about Crouzon Syndrome.
- EncephaloceleCao isExperienced. Learn about Encephalocele.
- Essential ThrombocythemiaCao isExperienced. Learn about Essential Thrombocythemia.
- Hearing LossCao isExperienced. Learn about Hearing Loss.
- Hermansky-Pudlak SyndromeCao isExperienced. Learn about Hermansky-Pudlak Syndrome.
- HerniaCao isExperienced. Learn about Hernia.
- HomocystinuriaCao isExperienced. Learn about Homocystinuria.
- Hypomelanotic DisorderCao isExperienced. Learn about Hypomelanotic Disorder.
- HypotoniaCao isExperienced. Learn about Hypotonia.
- Maple Syrup Urine DiseaseCao isExperienced. Learn about Maple Syrup Urine Disease.
- MenopauseCao isExperienced. Learn about Menopause.
- Methylmalonic AcidemiaCao isExperienced. Learn about Methylmalonic Acidemia.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Ocular AlbinismCao isExperienced. Learn about Ocular Albinism.
- Oculocutaneous AlbinismCao isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1
- Oculocutaneous Albinism Type 2
- Pendred SyndromeCao isExperienced. Learn about Pendred Syndrome.
- Platelet Storage Pool Deficiency
- PolydactylyCao isExperienced. Learn about Polydactyly.
- Retinopathy Pigmentary Mental Retardation
- Russell-Silver DwarfismCao isExperienced. Learn about Russell-Silver Dwarfism.
- Treacher Collins SyndromeCao isExperienced. Learn about Treacher Collins Syndrome.
- X-Linked Severe Combined Immunodeficiency