Charcot Marie Tooth (CMT)
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What is Charcot Marie Tooth (CMT) Disease?
Charcot Marie Tooth (CMT) disease is a group of inherited disorders that cause nerve damage. It is also called hereditary motor and sensory neuropathy.
CMT generally causes damage to the peripheral nerves in the arms and legs. It can result in muscle weakness, loss of sensation, difficulty walking, and foot deformities.
What Are the Symptoms of Charcot Marie Tooth Disease?
Symptoms vary based on the individual. As the disease progresses, they may spread from the legs and feet to the arms and hands. The most common symptoms include:
- Weakness in legs, ankles, and feet
- Loss of muscle bulk in legs and feet
- High foot arches
- Hammertoes – curled toes
- Decreased ability to run
- Footdrop – difficulty lifting foot at the ankle
- Higher than normal step
- Frequent tripping or falling
- Loss of feeling in legs and feet
What Causes Charcot Marie Tooth Disease?
CMT is a genetic condition. It is caused by mutations in the genes that affect the peripheral nerves. Because it is hereditary, you have a higher risk of developing the disease if someone in your immediate family has it.
UR Medicine's Treatments for Charcot Marie Tooth (CMT)
Beyond CMT, our Inherited Neuropathy Clinic at UR Medicine provides multidisciplinary care and opportunities for participation in research for children, adults, and families. We offer treatment for CMT and other forms of Inherited Neuropathy, including TTR Amyloid Polyneuropathy.
We focus on all aspects of disease including:
- Genetic confirmation
- Genetic and family counseling
- Gene therapy
- CMT and other inherited neuropathies
- Rehabilitation/Physical Therapy
- Access to research and clinical trials
- Orthotics
Cutting Edge Care with a Personal Touch
What Sets Us Apart?
Our mission is to provide excellent, specialized, multidisciplinary clinical care for patients and families with CMT and other forms of Inherited Neuropathy.
We work to improve the quality of life of our patients by providing a team of experts in different specialties needed to best care for Inherited Neuropathies, a friendly and supportive atmosphere, and coordinated care that is highly accessible for families.
We focus on all aspects of disease including diagnosis with genetic confirmation, genetic and family counseling, prevention and management of secondary symptoms and complications, access to clinical research studies and treatment trials and coordination of care with schools and other providers.
Our Team
- Jordan Bontrager, MS, CGC
Certified Genetics Counselor - Brooke McAdam, PT
Physical Therapist - Katy Eichinger, PhD, DPT
Physical Therapist and Clinical Evaluator for Clinical Trials
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Your donation, no matter the size, brings us closer to life-changing discoveries and treatments. For someone living with a neuromuscular disorder, your support means more than just hope – it means a chance at a fuller, more independent life.
Providers
Locations
We serve you in the Rochester metropolitan area and surrounding region.
1 location
Ambulatory Care Center at Strong Memorial Hospital
601 Elmwood Avenue, 1st Floor
Rochester, NY 14642