Dr. Yang Yanling
杨艳玲
Chief Physician; Professor; Doctoral Supervisor; Department of Pediatrics, Inherited Metabolic Disease and Neurogenetic Disorders Group
Where they practice, who they consult.
- Peking University First Hospital 北京大学第一医院, Beijing
- 30+ years in inherited metabolic and neurogenetic disease
- English, Mandarin
What they personally lead.
Training and recognition
Leads one of China's most-referred clinics for inherited metabolic diseases; standing committee member of the Chinese Medical Association Medical Genetics Branch (中华医学会医学遗传学分会) and the Pediatric Society Inherited Metabolic Disease Group; first or senior author on multiple Chinese expert consensus statements including the consensus on diagnosis and treatment of methylmalonic acidemia and the consensus on cobalamin C deficiency; long-running collaborative research on the Chinese mutation spectrum of MMACHC and other metabolic genes; PKU First Hospital is the historical reference center for the Department of Pediatrics in northern China and runs a high-volume neurogenetic clinic alongside the metabolic program
What to expect
Strong choice for a child with confirmed or suspected methylmalonic acidemia, propionic acidemia, urea cycle disorder, or unexplained metabolic encephalopathy. The clinic is heavily oversubscribed and runs primarily as a referral consultation rather than a primary-treatment service; bring all prior tandem mass spectrometry, urine organic acid, plasma amino acid, and acylcarnitine profiles, plus any prior gene panel results. International families should contact PKU First Hospital's international medical services in advance — outpatient registration without referral is difficult.
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