Education

• 2004.08

  Doctor of Medicine : Inha University

• 1998.02

  Master of Medicine : Inha University

• 1993.02

  Bachelor of Medicine : Inha University

Career

• 2024.05 ~ present

  Director of Rare Disease Management, Inha University Hospital

• 2002.01 ~ present

  Professor in Pediatrics, Inha University Hospital

• 2009.01 ~ 2010.01

  Visiting Professor, University of Utah

• 2001.01 ~ 2002.01

  Fellow in Pediatrics, Samsung Medical Center

• 1994.01 ~ 1998.01

  Resident in Pediatrics, Inha University Hospital

Professional Activities

• -

  Regular Member of the Asia Pacific Endocrine Society

• -

  Regular Member of The Korean Society for Bone and Mineral Research

• -

  Regular Member of the Korean Diabetes Association

• -

  Regular Member of The Korean Society of Medical Genetics and Genomics

• -

  Regular Member of The Korea Society of Inherited Metabolic Disease

• -

  Committe Member of The Korean Society of Lipid and Antherosclerosis Treatment Guideline

• -

  Auditor of the Association for Research of MPS and Rare Diseases

• -

  Editor of the Korean Society for The Study of Obesity

• -

  Director of Publication of the Korean Society of Pediatric Endocrinology

Honors

Research & Publications

• 2016

  Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study

• 2016

  Clinical Predictive Factors for Metabolic Syndrome in Obese Children and Adolescents

• 2016

  Prevalence and Relationships of Iron Deficiency Anemia with Blood Cadmium and Vitamin D Levels in Korean Women

• 2016

  The Diagnostic Value of Pelvic Ultrasound in Girls with Central Precocious Puberty

• 2016

  Early onset of puberty in an obese boy with Klinefleter syndrome

• 2016

  Diabetes-Specific Quality of Life of Korean children and adolescent with type 1 diabetes

• 2015

  Alternative biomarkers for assessing glycemic control in diabetes: fructosamine, glycated albumin, and 1,5-anhydroglucitol

• 2015

  Spinal Stenosis with Paraparesis in a Korean Boy with Albright's Hereditary Osteodystrophy: Identification of a Novel Nonsense Mutation in the GNAS

• 2014

  A Rare Diabetes Ketoacidosis in combined Severe Hypernatremic Hyperosmolarity in a new-onset Asian adolescent with type I diabetes