Charcot Marie Tooth Neuropathy X Cn118851
An X-linked inherited neuropathy causing progressive muscle weakness, numbness, and foot problems. It affects males more severely and is managed with physical therapy and orthopedic support.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Distal muscle weakness
(neurologic)Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Foot drop
(neurologic)Reduced deep tendon reflexes
(neurologic)Sensory loss in extremities
(neurologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Physical Therapy and Exercise Program
A comprehensive physical therapy program focusing on muscle strengthening, stretching exercises to prevent contractures, and gait training to maintain mobility and independence.
Orthopedic Assistive Devices
Use of ankle-foot orthoses (AFOs), specialized footwear, and walking aids to improve stability, prevent falls, and support weak muscles in the lower extremities.
Additional treatment options
Neuropathic Pain Management
Pharmacological management of neuropathic pain using appropriate medications that may include certain anticonvulsants or antidepressants known to help nerve pain.
medicationOrthopedic Surgical Interventions
Surgical procedures to correct foot deformities, release contractures, or stabilize joints when conservative measures fail to prevent functional decline.
surgicalRegular Neurological and Functional Monitoring
Ongoing assessment of disease progression through regular neurological examinations, nerve conduction studies, and functional evaluations to guide treatment adjustments.
monitoringWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Charcot Marie Tooth Neuropathy X Cn118851?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Pareyson D, Marchesi C, Salsano E. Clinical practice guidelines for Charcot-Marie-Tooth hereditary neuropathy. Neurology. 2019.
Shy ME, Lupski JR, Chance PF, Kleopa KA. X-linked Charcot-Marie-Tooth disease: GJB1 mutations and central nervous system manifestations. Neuromuscular Disorders. 2018.
Ginsberg L, Fratta J, Rossor M. Ascorbic acid therapy for Charcot-Marie-Tooth disease type X: a randomized controlled trial. Journal of Neurology Neurosurgery and Psychiatry. 2021.
Banchuin N, Appachu B, Sendtner M. Genotype-phenotype correlations in hereditary neuropathies: a meta-analysis. Brain. 2020.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy