01 · Personal genetics
Yuerkang
Childhood genetic health and development
Explore variants associated with single-gene disorders, together with drug-response and nutrition-related information, to support discussions between families and qualified professionals.
Who it is for
For newborns and their families. Applicable ages and individual tests are confirmed during consultation.
Service contents
Single-gene disorder screening
Covers selected blood, immune, endocrine, neurological, muscle, urinary and inherited metabolic conditions relevant to childhood genetic health.
Drug-response information
Reviews genetic differences associated with drug metabolism, efficacy or adverse reactions. Clinicians interpret these findings alongside age, medical conditions and other clinical information.
Constitution and nutrient metabolism
Interprets selected genetic information associated with nutrient metabolism and constitutional traits. The test list, evidence and reporting scope are agreed in the testing plan.
Report interpretation
Review reported variants, supporting evidence and the limits of interpretation. Findings that require further assessment should be discussed with qualified professionals using clinical information.
This service does not replace routine hospital newborn screening, pediatric examinations or clinical diagnosis.