Approach to Child Maltreatment
Published: Mar 27, 2025
This PedsCases note provides a one-page overview on approach to child maltreatment, including concerning features, investigations, management and guidance on reporting. It was created by Kayla Bailey, a medical student at the University of Alberta with help from Dr. Melanie Lewis, pediatrician at the University of Alberta and Dr. Jillian Popel and Dr. Erin Boschee, child maltreatment pediatricians at the University of Alberta.
Amniotic Band Syndrome
Published: Mar 19, 2025
This PedsCases note provides a one-page overview on amniotic band syndrome, including its pathophysiology, risk factors, presentation, diagnosis and management. It was created by Conné Lategan, a medical student at the University of Alberta with the help of Dr. Curtis Budden, Assistant Professor of Plastic Surgery at the University of Alberta.
Malaria
Published: Mar 09, 2025
This PedsCases note provides a one-page overview on pediatric malaria and its identification and management in Canada. It was created by Tina Madani Kia, a medical student at the University of Alberta with the help of Dr. Qaasim Mian, a pediatrician at the University of Alberta and Dr. Michael Hawkes, a pediatric infectious disease physician at the University of British Columbia.
Toddler's Diarrhea
Published: Feb 15, 2025
This PedsCases Note provides a one-page infographic on Toddler's Diarrhea. Toddler's diarrhea is characertized as benign chornic diarrhea in a well appearing toddler. It was created by Julia Craig with the help of Dr. Carrie Lewis
McCune Albright Syndrome
Published: Feb 10, 2025
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
Published: Feb 10, 2025
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)
Published: Feb 10, 2025
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
Published: Feb 10, 2025
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!
Alagille Syndrome
Published: Feb 10, 2025
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!
Klinefelter Syndrome
Published: Feb 10, 2025
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!