Your legacy can help bring an end to CMT. Learn how a planned gift can make an impact for generations to come.
CMT_Survivors_Guide
…Facebook. • Parents—Join the CMTA Parents Group on Facebook! • Youth—Join the CMTA Youth Group! • Follow us on Twitter. https://www.facebook.com/groups/CMTAssociation/ https://www.facebook.com/CMTAssociation https://www.cmtausa.org/index.php?option=com_content&view=article&id=149&Itemid=187 https://www.cmtausa.org/index.php?option=com_content&view=category&layout=blog&id=45&Itemid=171 https://www.youtube.com/watch?v=cKq6KwbDIWk https://www.cmtausa.org/index.php?option=com_content&view=category&layout=blog&id=42&Itemid=68 https://www.facebook.com/CMTAssociation https://www.facebook.com/groups/CMTAssociation/ https://www.facebook.com/groups/CMTAParents/ https://www.facebook.com/groups/CMTAYouth/…
Welcome to the Walk4CMT Toolbox
Welcome to the Walk4CMT Toolbox We are grateful that you have taken on a Walk 4 CMT event! This timeline will help you organize and promote your event, give you…
Pete Foley Joins CMTA Board of Directors
Glenolden, PA, June 21, 2021—The Charcot-Marie-Tooth Association (CMTA), the national patient advocacy organization leading CMT research, today announced the appointment of Pete Foley to its Board of Directors. Originally from…
Breakthrough Guide to Orthopedic Surgery for CMT
…comprehensive approach to CMT foot surgery. Dr. Glenn Pfeffer and orthopedic surgeons met to define standards for the surgical treatment of foot deformities resulting from CMT. We are incredibly proud…
2020_CMT_PFC_Pediatric_Neurology_transcript
…axonal form of CMT, CMT2, tend to progress a little bit faster than those with CMT1, but that’s just an average. There are certainly patients with CMT2 who stay about…
Voice_of_the_Patient_Report_8-19-2019
…PMP22 (CMT1A/HNPP), GJB1 (CMT1X), MFN2 (CMT2A), and MPZ (CMT1B). There are rarer forms of CMT that are autosomal recessive demyelinating motor and sensory neuropathies that include several genes categorized as…
CMT-and-Genetic-Testing-Why-Is-It-Important
…type of CMT is autosomal dominant demyelinating CMT, or CMT1. The most common genes in this type are PMP22 (CMT1A) and MPV (CMT1B). CMT2 refers to axonal CMT with autosomal…
CMTA Appoints Science and Technology Veteran, Patricia Verduin, PhD, to the Board of Directors
The Charcot-Marie-Tooth Association (CMTA), the largest philanthropic funder of Charcot-Marie-Tooth disease (CMT) research aimed at bringing treatments and a cure to patients, is pleased to announce the appointment of a…
The 2020 Winter CMTA Report
…see in the world of CMT. Be the Change: A Message from CEO Amy Gray Swimming Uphill with Jamal Hill CMTA Funds Cutting-Edge Gene Editing Studies for Type 2 CMT…
A New Treatment for CMT1A
…associations, including the CMTRF and the CMTA. DTx appreciates patient participation in natural history studies, such as the ongoing observational study ACT-CMT (Accelerate Clinical Trials in Charcot-Marie-Tooth Disease), which support…