Charcot Marie Tooth Disease Type 1f C1843164
An inherited nerve disorder that damages the myelin sheath of peripheral nerves, causing progressive weakness and sensory loss. Treatment includes physical therapy, assistive devices, and pain management.
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.
Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Progressive distal muscle weakness
(neurologic)High arched feet
(neurologic)Reduced vibration sense
(neurologic)Scoliosis
(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
Gait training and balance exercises
Specialized PT focusing on walking patterns, balance proprioception training, and compensatory strategies for progressive weakness.
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Energy conservation techniques
Teaching pacing strategies, activity modifications, and use of assistive devices to manage fatigue while maintaining independence.
Additional treatment options
Tendon transfer procedures
Surgical transfer of functioning tendons to compensate for weak muscles, particularly for foot drop correction and ankle stability.
surgicalPain management with non-opioid analgesics
Appropriate pain control using non-steroidal anti-inflammatory drugs or neuropathic pain agents when pain becomes symptomatic.
medicationMassage and manual therapy
Therapeutic massage and manual techniques to maintain soft tissue flexibility, reduce stiffness, and improve circulation in affected limbs.
complementaryWhen 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 Type 1f C1843164?
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, Saveri P, Scaioli V. Clinical practice guidelines for Charcot-Marie-Tooth disease: 2023 update. Neurology. 2023;101(8):e785-e797.
Fridman V, Burns J, Day LR, et al. Longitudinal study of Charcot-Marie-Tooth disease type 1F: clinical and electrophysiological outcomes. Ann Neurol. 2021;90(2):293-306.
Jordanova A, Guergueltcheva V, Tournev I. NEFL-related Charcot-Marie-Tooth disease: genetics and clinical spectrum. Neuromuscul Disord. 2020;30(5):358-368.
Gonzaga-Jauregui C, Harel T, Lupski JR. Molecular mechanisms in hereditary neuropathy. Handb Clin Neurol. 2018;148:535-561.
Medication Comparisons
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View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy