A plain-language guide

Charcot-Marie-Tooth disease type 1A

What's known, what's still uncertain, and what's actively debated, written plainly, and built only from published medical research.

Growing map · 32 sourced statements Every statement names its source Updated 2026-08-04
Please read this first. This guide is a companion to your medical team, not a replacement, and it is not medical advice. Everything here is tied to published research. If something you expected is not here, it almost always means we have not mapped a source for it yet, not that it is unknown to medicine. Charcot-Marie-Tooth disease type 1A is an early, growing map, so it will look incomplete on purpose: we would rather show less and have every line be something you can check than fill the page with claims we cannot stand behind. For anything about your own situation, your clinicians hold the full picture. How this guide is built and why.

What's Charcot-Marie-Tooth disease type 1A?

Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common inherited demyelinating disease of the peripheral nerves. It is caused by having an extra copy (a duplication) of the PMP22 gene, which the body uses to build the protective myelin coating around peripheral nerves.

Also indexed asOMIM:118220, MONDO:0007309
Features mapped16
Treatments mapped3
Published sources6
Last reviewed2026-08-04

Signs and symptoms

Foot dorsiflexor weakness

Weakness lifting the front of the foot (foot drop) is one of the most common first symptoms, which is why catching the toes and tripping can be an early sign.

Limited evidenceSource: PMID:41300731
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesOMIM:118220
Notesplain_language confirmed from PMID:41300731 via curation 2026-06-18 [claude (tier3 curation)]. | regrounded primary OMIM:118220 -> PMID:41300731 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Pes cavus

A high-arched foot (pes cavus) is a common feature and can become rigid enough to need surgery.

Limited evidenceSource: PMID:41300731
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:41981429, OMIM:118220
Notesplain_language confirmed from PMID:41981429 via curation 2026-06-12. | regrounded primary OMIM:118220 -> PMID:41300731 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Limb muscle weakness

Muscle weakness in CMT1A is symmetrical and affects the limbs farthest from the center of the body first, with the legs usually weaker and affected before the arms.

Limited evidenceSource: PMID:15239197
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:24646194, OMIM:118220
Notesplain_language confirmed from PMID:24646194 via curation 2026-06-25 [claude-draft]. | regrounded primary OMIM:118220 -> PMID:15239197 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Hammertoe

Hammer toes, where the toes curl downward, often occur alongside the high-arched foot.

Limited evidenceSource: PMID:41300731
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesOMIM:118220
Notesplain_language confirmed from PMID:41300731 via curation 2026-06-12. | regrounded primary OMIM:118220 -> PMID:41300731 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Insidious onset

CMT1A usually comes on gradually, most often in the first two decades of life, and is frequently first noticed as difficulty walking or running.

Limited evidenceSource: PMID:15239197
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:24646194, OMIM:118220
Notesplain_language confirmed from PMID:24646194 via curation 2026-06-25 [claude-draft]. | regrounded primary OMIM:118220 -> PMID:15239197 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Juvenile onset

Symptoms most often begin in the first two decades of life, frequently first noticed as difficulty walking or running.

Limited evidenceSource: PMID:10586223
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:24646194, OMIM:118220
Notesplain_language confirmed from PMID:24646194 via curation 2026-06-18 [claude (tier3 curation)]. | regrounded primary OMIM:118220 -> PMID:10586223 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Slowly progressive

CMT1A usually progresses slowly over many years. In adults the change can be gradual enough that it resembles ordinary ageing.

Limited evidenceCurated reference: OMIM:118220
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:24646194
Notesplain_language confirmed from PMID:24646194 via curation 2026-06-18 [claude (tier3 curation)].
Last reviewed2026-06-18

Peripheral neuropathy

The condition is a peripheral neuropathy: it affects the nerves serving the limbs, leading to weakness and reduced sensation in the feet and hands.

Limited evidenceSource: PMID:15239197
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:40635134, OMIM:118220
Notesplain_language confirmed from PMID:40635134 via curation 2026-06-12. | regrounded primary OMIM:118220 -> PMID:15239197 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Decreased motor nerve conduction velocity

On nerve testing, electrical signals travel more slowly than normal along the motor nerves. This slowing of conduction, measured during nerve testing, is a hallmark of the demyelinating form of CMT.

Limited evidenceSource: PMID:10586223
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:42246538, OMIM:118220
Notesplain_language confirmed from PMID:42246538 via curation 2026-06-18 [claude (tier3 curation)]. | regrounded primary OMIM:118220 -> PMID:10586223 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Distal sensory impairment

Many people also have reduced sensation in the feet and lower legs, because CMT1A affects the sensory nerves alongside the motor nerves.

Limited evidenceSource: PMID:15239197
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:24646194, OMIM:118220
Notesplain_language confirmed from PMID:24646194 via curation 2026-06-18 [claude (tier3 curation)]. | regrounded primary OMIM:118220 -> PMID:15239197 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Steppage gait

Weak ankle muscles cause a high-steppage gait, lifting the foot unusually high to avoid dragging the toes.

Limited evidenceCurated reference: OMIM:118220
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:42083783
Notesplain_language confirmed from PMID:42083783 via curation 2026-06-12.
Last reviewed2026-06-12

Hyporeflexia

Reflexes are reduced or absent, which a clinician can detect on examination.

Limited evidenceSource: PMID:15239197
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:41551139, OMIM:118220
Notesplain_language confirmed from PMID:41551139 via curation 2026-06-12. | regrounded primary OMIM:118220 -> PMID:15239197 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Autosomal dominant inheritance

CMT1A is inherited in an autosomal dominant pattern, meaning a single copy of the duplication is enough to cause it. It can also arise as a new (de novo) change in someone with no family history.

Limited evidenceSource: PMID:10586223
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:24646194, OMIM:118220
Notesplain_language confirmed from PMID:24646194 via curation 2026-06-18 [claude (tier3 curation)]. | regrounded primary OMIM:118220 -> PMID:10586223 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Distal amyotrophy

Along with weakness, the distal muscles waste and lose bulk over time (amyotrophy), with the legs typically affected before and more than the arms.

Limited evidenceSource: PMID:10586223
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:24646194, OMIM:118220
Notesplain_language confirmed from PMID:24646194 via curation 2026-06-18 [claude (tier3 curation)]. | regrounded primary OMIM:118220 -> PMID:10586223 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Distal muscle weakness

The muscles farther from the center of the body, especially in the lower legs and feet, tend to weaken. The legs are usually affected earlier and more severely than the arms.

Limited evidenceSource: PMID:10586223
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesPMID:24646194, OMIM:118220
Notesplain_language confirmed from PMID:24646194 via curation 2026-06-18 [claude (tier3 curation)]. | regrounded primary OMIM:118220 -> PMID:10586223 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

Kyphoscoliosis

Curvature of the spine (scoliosis or kyphosis) can occur in CMT1A, alongside other bone and muscle features such as a high-arched foot and hammer toes.

Limited evidenceSource: PMID:41300731
Evidence ratingweak
Study designontology_import
Confidence (0-1)0.7
Replicationunreplicated
Supporting sourcesOMIM:118220
Notesplain_language confirmed from PMID:41300731 via curation 2026-06-25 [claude-draft]. | regrounded primary OMIM:118220 -> PMID:41300731 on 2026-06-26 [Carrie Schluter, BCPA]
Last reviewed2026-06-26

How it is diagnosed

Charcot-Marie-Tooth disease, demyelinating, type 1A

Diagnosed using: PMP22 duplication genetic testing.

Limited evidenceSource: PMID:24646194
The source text this rests on
“Diagnosis is confirmed by finding respectively a PMP22 duplication, deletion or point mutation.”
An excerpt quoted verbatim from the source named above, shown as recorded. The full sentence is in the linked source.
Evidence ratingweak
Confidence (0-1)0.7
Replicationunreplicated
Notesconfirmed from PMID:24646194 via curation 2026-06-18
Last reviewed2026-06-18

Charcot-Marie-Tooth disease, demyelinating, type 1A

Diagnosed using: Nerve conduction study (electrophysiology).

Limited evidenceSource: PMID:24646194
The source text this rests on
“Electrophysiological evaluation is needed to determine whether the polyneuropathy is demyelinating.”
An excerpt quoted verbatim from the source named above, shown as recorded. The full sentence is in the linked source.
Evidence ratingweak
Confidence (0-1)0.7
Replicationunreplicated
Notesconfirmed from PMID:24646194 via curation 2026-06-18
Last reviewed2026-06-18

Charcot-Marie-Tooth disease, demyelinating, type 1A

Diagnosed using: Nerve sonography (ultrasound).

Limited evidenceSource: PMID:24646194
The source text this rests on
“Electrophysiological evaluation is needed to determine whether the polyneuropathy is demyelinating. Sonography of the nerves can be useful.”
An excerpt quoted verbatim from the source named above, shown as recorded. The full sentence is in the linked source.
Evidence ratingweak
Confidence (0-1)0.7
Replicationunreplicated
Notesconfirmed from PMID:24646194 via curation 2026-06-25
Last reviewed2026-06-25

Treatment and management

What the research describes, not a recommendation. Treatment decisions belong with your clinician.

This covers treatments that appear in the published research mapped here. Investigational and experimental therapies are not included, so their absence is a boundary of this map, not a sign they do not exist.

Orthotic devices for foot and ankle

Orthotic devices, such as braces fitted to the foot and ankle, are used to manage the foot and ankle deformities of CMT. They support walking but do not change the underlying nerve condition.

Used to help with: Charcot-Marie-Tooth disease, demyelinating, type 1A.

Limited evidenceSource: PMID:37147931
The source text this rests on
“Orthotic devices may be prescribed for the management of foot and ankle deformities caused by Charcot-Marie-Tooth disease (CMT).”
An excerpt quoted verbatim from the source named above, shown as recorded. The full sentence is in the linked source.
Evidence ratingweak
Confidence (0-1)0.7
Replicationunreplicated
Notesconfirmed from PMID:37147931 via curation 2026-06-25
Last reviewed2026-06-25

Physical, occupational and rehabilitation therapy

There is no drug that changes the course of CMT1A, so care is supportive and aimed at symptoms. It can involve a rehabilitation physician, a physiotherapist and an occupational therapist working together.

Used to help with: Charcot-Marie-Tooth disease, demyelinating, type 1A.

Limited evidenceSource: PMID:24646194
The source text this rests on
“Treatment is currently symptomatic and may include management by a rehabilitation physician, physiotherapist, occupational therapist and orthopaedic surgeon.”
An excerpt quoted verbatim from the source named above, shown as recorded. The full sentence is in the linked source.
Evidence ratingweak
Confidence (0-1)0.7
Replicationunreplicated
Notesconfirmed from PMID:24646194 via curation 2026-06-25
Last reviewed2026-06-25

Orthopaedic surgery

An orthopaedic surgeon may be part of the care team for CMT1A, for example to correct foot deformities that affect walking.

Used to help with: Charcot-Marie-Tooth disease, demyelinating, type 1A.

Limited evidenceSource: PMID:24646194
The source text this rests on
“…may include management by a rehabilitation physician, physiotherapist, occupational therapist and orthopaedic…”
An excerpt quoted verbatim from the source named above, shown as recorded. The full sentence is in the linked source.
Evidence ratingweak
Confidence (0-1)0.7
Replicationunreplicated
Notesconfirmed from PMID:24646194 via curation 2026-06-25
Last reviewed2026-06-25

What changes how it shows up

Carrying the genetic change is not the whole story. The factors below are described in the research mapped here as changing whether, or how strongly, the condition appears. They modulate how the genotype is expressed; they do not, on their own, cause or cure it.

PMP22 duplication (17p12)

CMT1A is caused by a duplication of the PMP22 gene on chromosome 17 (a 17p12 duplication), meaning the person carries an extra copy of this region.

Described as modulating: Charcot-Marie-Tooth disease, demyelinating, type 1A.

Limited evidenceSource: PMID:41300731
The source text this rests on
“…most commonly Charcot-Marie-Tooth type 1A (CMT1A; 17p12…”
An excerpt quoted verbatim from the source named above, shown as recorded. The full sentence is in the linked source.
Evidence ratingweak
Confidence (0-1)0.7
Replicationunreplicated
Notesconfirmed from PMID:41300731 via curation 2026-06-25
Last reviewed2026-06-25

How to read the evidence labels

Widely acceptedSpecialists broadly agree on this.
Strong evidenceBacked by solid, repeated research.
Moderate evidenceReasonable evidence, still being confirmed.
Limited evidenceSome evidence, but not yet convincing.
Early evidenceAn early finding that needs more study.
Experts disagreeResearchers actively disagree about this.
No longer supportedLater, stronger evidence or guidance overturned this.

Where this comes from

This guide is built from 6 published source(s). Every claim above links back to one of them. Click any source ID to read the original on PubMed.

OMIM:118220 · Orphanet/HPO annotations for Charcot-Marie-Tooth disease, demyelinating, type 1A
PMID:10586223 · Overview of Charcot-Marie-Tooth disease type 1A.
PMID:15239197 · Charcot-Marie-Tooth disease type 1A: a clinical, electrophysiological, pathological, and genetic study.
PMID:24646194 · PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Pal
PMID:37147931 · Relationship between care pathway features and use or non-use of orthotic devices by individuals with Charcot-Marie-Toot
PMID:41300731 · PMP22-Related Neuropathies: A Systematic Review.

Take it further

Printed, source-linked documents built from this condition's graph — ready to bring to an appointment or attach to a coverage request. Every claim carries its published source, the same as this guide.