iatroX logo
brainstormaskiatroX
knowledge centreblog
Knowledge Centre / Charcot-Marie-Tooth Disease

Charcot-Marie-Tooth Disease

Overview of hereditary motor and sensory neuropathy.

Reviewed by Dr Kola Tytler MBBS CertHE MBA MRCGP (General Practitioner)
Last reviewed: 21 October 2025
NeurologyGenetics

Clinical Guidelines

A Consensus Statement on the Surgical Treatment of Charcot-Marie-Tooth Disease (Foot Ankle Int. 2020)
National
Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease (JNNP 2022)
National
Clinical practice guidelines for the diagnosis and management of Charcot-Marie-Tooth disease (Neurologia 2025)
National
A Consensus Statement on the Surgical Treatment of Charcot-Marie-Tooth Disease
Local
Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease
Local
Clinical practice guidelines for the diagnosis and management of Charcot-Marie-Tooth disease
Local

Recent iatroX Q&As

  • What are the key clinical features to consider when diagnosing Charcot-Marie-Tooth Disease in a patient presenting with motor and sensory symptoms?Updated: 8/17/2025
  • Which genetic tests are recommended for confirming a diagnosis of Charcot-Marie-Tooth Disease in primary care?Updated: 8/17/2025
  • What are the current guidelines for the referral of patients with suspected Charcot-Marie-Tooth Disease to specialist services?Updated: 8/17/2025
askiatroX
privacytermshow it workscpdinsights
Download on the App StoreGet it on Google Play