| Specialists | Doctor |
|---|---|
| Genetic counseling, genetic diagnosis and management (Inborn Error of Metabolism, Multiple Congenital Malformation, Chromosome anomaly, newborn screen disorders (except G6PD deficiency), Huntington's disease, Spinocerebellar atrophy) | Wuh-Liang Hwu, Yin-Hsiu Chien, Ni-Chung Lee |
| Prenatal invasive procedure (Chorionic villus sampling, amniocentesis, cord blood sampling) | Hsiao-Lin Hwa, Shin-Yu Lin,Jessica Kang, Ming-Chen |
| Molecular and cytogenetic analysis for chromosome disorder and certain genetic disorders | Ming-Chen |
| Paternity test (for parents and child, grandparents and grandchild, and sibling testing) | Hsiao-Lin Hwa, Shin-Yu Lin,Jessica Kang, Wuh-Liang Hwu |
| G6PD deficiency (Newborn screen) | Ni-Chung Lee |
| Pre-implantation genetic diagnosis, Intrauterine fetal therapy | Ming-Chen |
| Neurogenetic diseases (including NF1 and NF2, Familial Alzheimer Disease and Parkinson's Disease, Motor Neuron Disease and Amyotrophic Lateral Sclerosis, Autosomal dominant noctural frontal lobe epilepsy etc) | Ming-Jen Lee |
| Gene Therapy | Wuh-Liang Hwu |
| Treatment for lysosomal storage disease | Yin-Hsiu Chien |
| Adult Genetic Disease (Endocrinology disorders) | Pei-Lung Chen |
| Cancer gene diagnosis | Po-Han Lin |
| Tuberous sclerosis complex (TSC) | Pei-Lung Chen |
| Down syndrome | Ni-Chung Lee |
| Congenital inherited arrhythmia syndrome (Long QT syndrome, Brugada syndrome, Short QT syndrome, Early repolarization syndrome, Idiopathic Ventricular tachycardia or fibrillation, hypertrophic cardiomyopathy) | Jyh-Ming Juang |
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