The essential podcasts you need to listen to!
Pediatric Education Online
The essential podcasts you need to listen to!
We're developing a new website and need your feedback!
We have a new slogan!
McCune Albright Syndrome
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Wiskott-Aldrich Syndrome
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Neurofibromatosis Type 1 (NF1)
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Tuberous Sclerosis Complex
Explore this comprehensive series of 14 PedsCases notes on common pediatric genetic syndromes, including Fragile X, Rett, Beckwith-Wiedemann, Prader-Willi, Williams, Marfan, DiGeorge, Noonan, Klinefelter, Alagille, Tuberous Sclerosis Complex, Neurofibromatosis Type 1, McCune-Albright, and Wiskott-Aldrich. Created by Dr. Katharine Jensen, Pediatric Resident at the University of Alberta, with expert guidance from Dr. Karen Forbes, Professor of Pediatrics and Hospitalist at the University of Alberta. A valuable resource for understanding key genetic syndromes in pediatrics!
Proudly sponsored by the Canadian Paediatric Society, University of Alberta Medical Students' Association, and the University of Alberta Department of Pediatrics:
