The division of Pediatric Genetics, Endocrinology and Metabolism was set up on 2003, which provide clinical diagnosis, specific genetic tests including chromosome study and molecular genetic diagnosis, endocrine tests and inherited metabolic disorders for children and genetic counseling for rare disease. 

The medical services include:

1. Provide diagnosis, treatments, genetic counseling and family support about genetic diseases, rare diseases and inherited metabolic diseases..

2. Provide specific tests and excellent cares for pediatric endocrinologic diseases - congenital hypothyroidism, hyperthyroidism, IDDM, congenital adrenal hyperplasia, growthhormone deficiency, precocious puberty and gonadal disorder.

3. Provide confirmation and treatment for inherited metabolic disorders.

4. Provide specific diagnosis and molecular genetic diagnosis for rare diseases via National Health Bureu to National Medical Center for confirmation.

5. Provide special training program of Genetics, Endocrine and Metabolism for Pediatrics.