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Diagnosing CMT - Charcot–Marie–Tooth Association No, genetic testing is not required to diagnose CMT A clinical diagnosis based on symptoms, nerve conduction study (NCS) results, and family history can determine whether someone has CMT
CMT-SORD - Sorbitol Dehydrogenase (SORD) Deficiency | CMTA In CMT-SORD, sorbitol levels are very high in urine and can confirm a suspected CMT-SORD diagnosis The company reports that this sponsored testing is available at no cost to patients and caregivers who qualify, removing potential barriers to diagnosis, care management, and future treatment
Genetics of CMT - Charcot–Marie–Tooth Association Shawna Feely, Certfied Genetics Counselor and CMTA Advisory Board Member, provides an in-depth look at the genetics of cmt, including family history, genetic testing and reproductive options
What is HNPP? - Charcot–Marie–Tooth Association This finding should prompt physicians to seek the diagnosis and perform DNA testing DNA testing allows physicians to reach a definitive diagnosis if the loss of one copy of PMP22 is found
CMTA Centers of Excellence | Expert Care for CMT Find specialized care for CMT at CMTA Centers of Excellence Learn how expert teams deliver diagnosis, treatment, and research opportunities worldwide
What’s New in CMT: Update from CMTA-STAR’s Davide Pareyson, MD While no FDA-approved treatments exist, advancements in genetic testing, rehabilitation strategies, surgical approaches, and CMTA-STAR-driven treatment research continue to move the field forward
What Is CMT? - Charcot–Marie–Tooth Association Registering today ensures you stay informed about the latest developments in CMT research You’ll also be the first to know about any clinical trial or study you wish to participate in Registration is free, secure, and open to everyone with CMT, no matter where you are in your journey