FAQs

What is CMT2A?

CMT2A is a genetic nerve disorder affecting muscle strength.

What causes CMT2A?

It’s caused by mutations in the MFN2 gene, impacting nerve function.

What symptoms should I expect?

Symptoms include muscle weakness, foot deformities, and difficulty walking.

How is CMT2A diagnosed?

Diagnosis involves genetic testing and nerve conduction studies.

Is there a treatment?

While no cure exists, therapies help manage symptoms effectively.

Charcot-Marie-Tooth

Understanding Type 2A: Symptoms, Causes, and Support

CMT 2A

Images/ videos showing symptoms and nerve biopsy results.