Overview
Xin Fan practices in Nanning, China. Ms. Fan is rated as an Experienced expert by MediFind in the treatment of Micrognathia. Her top areas of expertise are Congenital Hypothyroidism, Short Philtrum, Neonatal Hypothyroidism, and Short Stature (Growth Disorders).
Her clinical research consists of co-authoring 89 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 Micrognathia.
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
- Distinguished
- Congenital HypothyroidismMs. Fan isDistinguished. Learn about Congenital Hypothyroidism.
- Neonatal HypothyroidismMs. Fan isDistinguished. Learn about Neonatal Hypothyroidism.
- Short PhiltrumMs. Fan isDistinguished. Learn about Short Philtrum.
- Advanced
- Carnitine-Acylcarnitine Translocase Deficiency
- HypothyroidismMs. Fan isAdvanced. Learn about Hypothyroidism.
- Jacobsen SyndromeMs. Fan isAdvanced. Learn about Jacobsen Syndrome.
- Short Stature (Growth Disorders)
- Trisomy 14 MosaicismMs. Fan isAdvanced. Learn about Trisomy 14 Mosaicism.
- Experienced
- Achalasia Microcephaly SyndromeMs. Fan isExperienced. Learn about Achalasia Microcephaly Syndrome.
- AcrocephalopolydactylyMs. Fan isExperienced. Learn about Acrocephalopolydactyly.
- Acromesomelic DysplasiaMs. Fan isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type