Charcot–Marie–Tooth disease (CMT) is a hereditary motor and sensory neuropathy of the peripheral nervous system characterized by progressive loss of muscle tissue and touch …

Jan 23, 2025 · Describe the clinical characteristics of CMT hereditary neuropathy; 2. Review the causes of CMT hereditary neuropathy; 3. Provide an evaluation strategy to identify the cause …

Inherited neuropathies known as Charcot-Marie-Tooth (CMT) disease are genetically heterogeneous disorders affecting the peripheral nerves, causing significant and slowly …

The CMTA is a nonprofit organization aimed at improving the lives of those impacted by CMT. Learn more and donate to help us create a world without CMT.

What is pediatric Charcot-Marie-Tooth disease (CMT)? Charcot-Marie-Tooth (CMT) disease is a neurological (nerve) disorder that causes a child to lose feeling and movement in their legs, …

The Charcot-Marie-Tooth (CMT) Center at the Johns Hopkins Hospital offers comprehensive evaluations and symptom management for patients with confirmed or suspected CMT disease.

There currently are no available treatments that act to slow the progression of Charcot-Marie-Tooth disease. There are promising CMT research studies that indicate that this may change …

Charcot-Marie-Tooth (CMT) is an inherited neuromuscular disease that causes nerves to malfunction. This condition affects the peripheral nerves responsible for voluntary muscle …

Charcot-Marie-Tooth disease is a group of inherited disorders caused by a mutation in genes. It affects movement and feeling in the arms and legs.

Jan 17, 2025 · Charcot-Marie-Tooth (CMT) disease, also known as hereditary motor and sensory neuropathy (HMSN), refers to a heterogeneous group of inherited peripheral neuropathies …