Charcot-Marie-Tooth Disease

Sponsored diagnostic testing programs for Charcot-Marie-Tooth Disease

Charcot-Marie-Tooth disease is a group of hereditary motor and sensory neuropathies causing progressive distal weakness, muscle wasting, sensory loss, and foot deformities. Age of onset and severity vary widely depending on the genetic subtype. Genetic testing clarifies the subtype, guides prognosis, and supports counseling.

1 program found for Charcot-Marie-Tooth Disease

Programs

1 program
Invitae Unlock™

Invitae Inherited Retinal Disorders Panel

This program offers U.S. clinicians access to comprehensive genetic testing for patients with suspected inherited retinal diseases, including RP, CRD, LCA, Stargardt disease, and other IRDs. Testing is also appropriate for asymptomatic individuals with a family history of IRD or a known pathogenic variant in a relevant gene, supporting diagnosis, risk assessment, and patient management.

Ophthalmology
ViewOrder
Performing labInvitae | Labcorp