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!

Click the image below for a full-page PDF. 

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References

1. Kliegman, R. M., Stanton, B. F., St. Geme, J. W., Schor, N. F., & Behrman, R. E. (Eds.). (2022). Nelson Textbook of Pediatrics (21st ed.). Elsevier.