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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/…
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…
CMTA Spring 2024 Report: Progress and Impact that Empowers Communities
The 2024 Spring CMTA Report (756 downloads ) VIEW IN BROWSER Sue Bruhn, the CEO of CMTA, expresses gratitude and excitement for the upcoming year and highlights the achievements and…
Preguntas Frecuentes
…Tooth. ¿Hay algún tratamiento para CMT? No hay tratamientos conocidos que detenga o disminuya la progresión del CMT, pero la CMTA está financiando investigaciones para encontrar tratamientos. La terapia física,…
The Differences Between Charcot-Marie-Tooth Disease and Muscular Dystrophy (MD): An Overview
…No, CMT is not a form of MD. Although CMT shares many symptoms with the many forms of MD, CMT is a disease of the peripheral nerves and MD is…
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…
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…
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…
CMT2S Breakthrough
…marks a significant step forward for community members who have CMT2S. CMT2S is a very rare and often debilitating autosomal recessive type of CMT. A potential treatment for CMT2S, Vanda’s…