![Charcot-Marie-Tooth Association on Twitter: "Charcot-Marie-Tooth disease (CMT) is a form of hereditary peripheral neuropathy that can cause progressive loss of sensation and function in hands, arms, legs, and feet. Learn more: https://t.co/fmVGUk3K4o # Charcot-Marie-Tooth Association on Twitter: "Charcot-Marie-Tooth disease (CMT) is a form of hereditary peripheral neuropathy that can cause progressive loss of sensation and function in hands, arms, legs, and feet. Learn more: https://t.co/fmVGUk3K4o #](https://pbs.twimg.com/media/FL2BkviXMAATR7Y.png)
Charcot-Marie-Tooth Association on Twitter: "Charcot-Marie-Tooth disease (CMT) is a form of hereditary peripheral neuropathy that can cause progressive loss of sensation and function in hands, arms, legs, and feet. Learn more: https://t.co/fmVGUk3K4o #
![Confirmation of the GNB4 gene as causal for Charcot–Marie–Tooth disease by a novel de novo mutation in a Czech patient - Neuromuscular Disorders Confirmation of the GNB4 gene as causal for Charcot–Marie–Tooth disease by a novel de novo mutation in a Czech patient - Neuromuscular Disorders](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/6e6c7aaf-5cb4-4c03-b7a0-61acafd4a078/nmd3254-fig-0001_lrg.jpg)
Confirmation of the GNB4 gene as causal for Charcot–Marie–Tooth disease by a novel de novo mutation in a Czech patient - Neuromuscular Disorders
![Images of bone disorders in Charcot-Marie-Tooth syndrome. | Download High-Resolution Scientific Diagram Images of bone disorders in Charcot-Marie-Tooth syndrome. | Download High-Resolution Scientific Diagram](https://www.researchgate.net/publication/339325328/figure/fig3/AS:859836308783105@1582012359316/Images-of-bone-disorders-in-Charcot-Marie-Tooth-syndrome.png)
Images of bone disorders in Charcot-Marie-Tooth syndrome. | Download High-Resolution Scientific Diagram
![A very mild phenotype of Charcot-Marie-Tooth disease type 4H caused by two novel mutations in FGD4 - ScienceDirect A very mild phenotype of Charcot-Marie-Tooth disease type 4H caused by two novel mutations in FGD4 - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022510X1930231X-gr1.jpg)
A very mild phenotype of Charcot-Marie-Tooth disease type 4H caused by two novel mutations in FGD4 - ScienceDirect
![Surgical outcomes of cavovarus foot deformity in children with Charcot-Marie-Tooth disease - Neuromuscular Disorders Surgical outcomes of cavovarus foot deformity in children with Charcot-Marie-Tooth disease - Neuromuscular Disorders](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/c6eff597-87fe-4baa-a250-d5675c97d77d/gr1.jpg)