Charcot Marie Tooth Disease X Linked Recessive 4 C0795910
An X-linked form of inherited nerve disease that causes muscle weakness and sensory loss, mainly in males. Treatment involves rehabilitation and mobility assistance.
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 (lower limbs)
(neurologic)Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Foot drop
(neurologic)Pes cavus (high-arched feet)
(neurologic)Hand weakness (distal upper limb)
(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
Comprehensive Physical Therapy Program
A structured physical therapy program focusing on muscle strengthening, stretching exercises, and balance training to maintain motor function and prevent contractures in Charcot-Marie-Tooth disease.
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Assistive Devices and Orthotics
Use of ankle-foot orthoses (AFOs), specialized footwear, and assistive devices such as canes or walkers to improve mobility, prevent falls, and support foot drop in X-linked CMT4.
Additional treatment options
Orthopedic Surgery for Foot Deformities
Surgical intervention to correct severe pes cavus, hammertoes, or ankle instability that do not respond to conservative management in moderate CMT4.
surgicalNeuropathic Pain Management
Pharmacological management of neuropathic pain using first-line agents such as gabapentin or pregabalin, titrated appropriately for symptom relief in CMT patients.
medicationRegular Neurological Monitoring
Ongoing neurological assessments including nerve conduction studies, muscle strength evaluation, and functional mobility tracking to monitor disease progression and adjust treatment plans.
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 Disease X Linked Recessive 4 C0795910?
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.
Shy ME, Patzkı A, Laura M, et al. Consensus in Practice: Guidelines for the Management of Charcot-Marie-Tooth Disease and Related Hereditary Neuropathies. Neurology. 2022.
Brennan KM, Zuchner S. Hereditary Motor and Sensory Neuropathies: Understanding CMTX4 and Related Conditions. Nat Rev Neurol. 2021.
Pareyson D, Saveri P, Pisciotta C, et al. Longitudinal Study of Patients with X-Linked Charcot-Marie-Tooth Disease Type 4. Brain. 2020.
Hattori N, Kumamoto K, Ichinose Y, et al. Genotype-Phenotype Correlations in Charcot-Marie-Tooth Hereditary Neuropathy: A Systematic Review and Meta-Analysis. J Neurol Neurosurg Psychiatry. 2023.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy