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!

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!

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!

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!