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DTSTART;TZID=America/Toronto:20260116T110000
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DTSTAMP:20260627T094418
CREATED:20260108T171407Z
LAST-MODIFIED:20260108T174653Z
UID:10000115-1768561200-1768564800@ccmg.51-222-78-205.ygkweb.ca
SUMMARY:TeleGraf
DESCRIPTION:About this series – Telehealth for Genetics Residents and Fellows. A monthly teaching session brought to you by the members of the RCPSC Specialty Committee in Medical Genetics. \nTo register\, click the button below or go to https://us06web.zoom.us/webinar/register/WN_2LAO5jlHSQ-WA_xonc9ouA. \n \n  \n  \n  \n  \n2025-2026 TeleGraf from 11:00am – 12:00pm ET on:\nFriday\, January 16\, 2026\nReview and Update of the Ehlers-danlos Syndromes (EDS) and the Hypermobility Spectrum Disorders (HSD) \nWe will review the last classification of Ehlers-Danlos syndromes (EDS) by the International Consortium on EDS (2017)\, describing 13 types (a fourteenth added since) and their genetic etiology. The diagnostic criteria of the most frequent type\, hypermobile Ehlers-Danlos syndrome (hEDS)\, and of the hypermobility spectrum disorders (HSD) will be presented. hEDS is an exception in that it clusters in families in a dominant fashion\, but no known single gene is associated. We will review the recent genomic studies of this complex multisystemic and multifactorial disorder and possible overlapping mechanisms with HSD. Finally\, we will review the numerous co-existing conditions with EDS\, particularly with hEDS\, demonstrating the multisystemic and variable expression of this disorder. \nLearning Objectives: \n\nIdentify the 14 types of Ehlers-Danlos syndromes (EDS) and their genetic etiology.\nDiagnose the frequent type\, Ehlers-Danlos hypermobile type (hEDS)\, and the hypermobility spectrum disorders (HSD).\nRecognize the various conditions co-existing with EDS demonstrating its multisystemic nature and variable expression.\n\nSpeaker: Dr. Gail Ouellette \nGail Ouellette has a PhD. in molecular genetics (Université de Montréal) and MSc. in genetic counselling (McGill University). She was the founding-president of the Regroupement québécois des maladies orphelines\, RQMO. She established the RQMO’s iRARE Centre and its EDS Support Centre. She has recently founded the Canadian iRARE Centres. Gail Ouellette is a member of the Board of Directors of the Groupe d’étude et de recherche sur le syndrome d’Ehlers-Danlos (GERSED\, France) and is a medical advisor for the EDS Canada Foundation. She has obtained training on EDS through the EDS Canada Foundation’s annual education conferences and through the EDS Society’s international symposiums and ECHO programs for health professionals\, including the continuing ECHO Genetics & Genomics program. She has taught courses on the molecular and genetic aspects of EDS as part of the University Certificate on Ehlers-Danlos syndrome offered by the Faculty of Medicine of Université Paris-Est (Créteil). \nFriday\, February 20\, 2026\nFriday\, March 20\, 2026 – Tentative\nFriday\, April 17\, 2026\nFriday\, May 15\, 2026\nFriday\, June 19\, 2026
URL:https://ccmg.51-222-78-205.ygkweb.ca/event/telegraf-4-4/
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