Just diagnosed with Charcot-Marie-Tooth disease, type I?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Charcot-Marie-Tooth disease, type I, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Charcot-Marie-Tooth disease, type I hub →Overview
Charcot-Marie-Tooth disease, type I is a rare condition. Also known as Autosomal dominant demyelinating Charcot-Marie-Tooth disease, CMT1, Charcot-Marie-Tooth neuropathy type 1, Hereditary motor and sensory neuropathy type 1. Tomeko brings together the specialists, research, clinical trials, treatments and community for Charcot-Marie-Tooth disease, type I so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:65753 · GARD 0012433
Find care for Charcot-Marie-Tooth disease, type I
Authoritative references for Charcot-Marie-Tooth disease, type I
Research & market landscape for Charcot-Marie-Tooth disease, type I
Following Charcot-Marie-Tooth disease, type I for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Charcot-Marie-Tooth disease, type I — the real-world landscape behind the condition, in one place.
- Latest Charcot-Marie-Tooth disease, type I research on PubMed ↗
- Recruiting Charcot-Marie-Tooth disease, type I trials on ClinicalTrials.gov ↗
- Explore the Charcot-Marie-Tooth disease, type I research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Charcot-Marie-Tooth disease, type I and every rare condition. See how Tomeko works with industry →
Common questions
What is Charcot-Marie-Tooth disease, type I?
Charcot-Marie-Tooth disease, type I is a rare condition. Also known as Autosomal dominant demyelinating Charcot-Marie-Tooth disease, CMT1, Charcot-Marie-Tooth neuropathy type 1, Hereditary motor and sensory neuropathy type 1. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Charcot-Marie-Tooth disease, type I together in one place.
What are the symptoms of Charcot-Marie-Tooth disease, type I?
Symptoms of Charcot-Marie-Tooth disease, type I vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Charcot-Marie-Tooth disease, type I.
How is Charcot-Marie-Tooth disease, type I treated?
Treatment for Charcot-Marie-Tooth disease, type I depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Charcot-Marie-Tooth disease, type I, and review current options with them.
What causes Charcot-Marie-Tooth disease, type I — is it genetic?
The cause and inheritance of Charcot-Marie-Tooth disease, type I are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Charcot-Marie-Tooth disease, type I can explain what it means for you and your family.
I was just diagnosed with Charcot-Marie-Tooth disease, type I — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Charcot-Marie-Tooth disease, type I, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Charcot-Marie-Tooth disease, type I?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Charcot-Marie-Tooth disease, type I, filtered to your area.
Are there clinical trials for Charcot-Marie-Tooth disease, type I?
Tomeko shows live, recruiting studies for Charcot-Marie-Tooth disease, type I from ClinicalTrials.gov on the hub.
Related conditions
Other conditions on Tomeko you may be looking for:
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- Charcot-Marie-Tooth disease, type IA
- Charcot-Marie-Tooth disease, Guadalajara neuronal type
- Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome
- Charcot-Marie-Tooth disease, dominant intermediate G
- CHARGE syndrome
- Charcot-Marie-Tooth disease, dominant intermediate A
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