Newborn Screening (Archived)
Activity
Large Group Session
Large Group Session
Part 1: What are genetic metabolic disorders? General approach to diagnosis, treatment (MCAD as example (Multiple Acyl Coenzyme A Dehydrogenase Deficiency)). Part 2: Newborn screening overview. Basic principles of screening. Screening for metabolic disorders. Newborn screening: recent advances and trends worldwide; Screening in Ontario; Ethical issues and challenges.
Curriculum Block
Part 3
- Indicates most relevant
Tags
Archived
Archived
Basic Sciences
Biochemistry
Human development
Metabolism
Prevention and control
Reproduction
Cohort Year
2010
Curriculum Block
Part 3
Curriculum Week
Part 3
Discipline
Genetics
Pediatrics
MCC Presentations
Glucose Abnormalities
Newborn Assessment
MeSH
Amino Acid Metabolism, Inborn Errors [C16.320.565.100]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Molecular Biology [H01.158.273.343.595]
Multiple Acyl Coenzyme A Dehydrogenase Deficiency [C16.320.565.100.614]
Neonatal Screening [E01.370.500.580]
