Prader Willi Syndrome
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X,
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X,
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X,
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X,
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X,
This video is the second in a two-part series that presents an approach to family history and pedigree. In this video, viewers will review the classic patterns of Mendelian inheritance and see how these patterns might look in a pedigree. This podcast was developed by Erinna McMurtry and Jovana Miladinovic in collaboration with Dr. Patricia Blakley, an Associate Professor at the Department of Pediatrics at the University of Saskatchewan with specialization in clinical genetics and developmental pediatrics.
This video presents an overview of genetic testing technologies. This is part 3 of a 3-part series on genetic disorders. This episode will describe four types of genetic testing technologies, describe the advantages and disadvantages of direct-to-consumer genetic testing, and discuss personalized medicine. This podcast was developed by Rozlyn Boutin a senior medical student at the University of British Columbia, in collaboration with Dr. Caitlin Chang, a medical geneticist at the British Columbia Children’s Hospital in Vancouver.
This video presents an overview of X-linked inheritance. This is part 2 of a 3 part series on genetic disorders. This episode will define X-linked inheritance and describe dosage compensation using a case of X-linked hypophosphatemia as an example. This video was developed by Rozlyn Boutin a senior medical student at the University of British Columbia, in collaboration with Dr. Caitlin Chang, a medical geneticist at the British Columbia Children’s Hospital in Vancouver
This video discusses long QT syndrome as an example to discuss medical conditions that are inherited in an autosomal dominant fashion. This is the first video in a 3-video series on Genetic Diseases. It was created by Dr. Rozlyn Boutin, a resident at British Columbia’s Children’s Hospital in Vancouver, BC, Canada in collaboration with Dr. Caitlin Chang, a medical geneticist at BC Children’s.
This podcast will provide listeners with an understanding of Maple Syrup Urine Disease, its clinical signs and symptoms, and management. This podcast was developed by fourth year medical student Angela Messer in collaboration with Dr. Shailly Jain, an Associate Professor in the Department of Medical Genetics at the University of Alberta.