CANOMAD syndrome: Introduction
CANOMAD syndrome: A rare syndrome characterized by a range of abnormalities caused by immune-mediated nerve demyelination. There is usually no loss of limb function associated with the disorder. The face, throat, mouth and eye symptoms (weakness of the muscles) usually come and go.
More detailed information about the symptoms,
causes, and treatments of CANOMAD syndrome is available below.
Symptoms of CANOMAD syndrome
See full list of 13
symptoms of CANOMAD syndrome
Treatments for CANOMAD syndrome
Read more about treatments for CANOMAD syndrome
Home Diagnostic Testing
Home medical testing related to CANOMAD syndrome:
- Nerve Neuropathy: Related Home Testing:
Wrongly Diagnosed with CANOMAD syndrome?
Causes of CANOMAD syndrome
Read more about causes of CANOMAD syndrome.
Less Common Symptoms of CANOMAD syndrome
Read more about symptoms of CANOMAD syndrome
CANOMAD syndrome: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and CANOMAD syndrome
Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency
is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple...read more »
Read more about Misdiagnosis and CANOMAD syndrome
CANOMAD syndrome: Research Doctors & Specialists
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
Evidence Based Medicine Research for CANOMAD syndrome
Medical research articles related to CANOMAD syndrome include:
Click here to find more evidence-based articles on the TRIP Database
Research about CANOMAD syndrome
Visit our research pages for current research about CANOMAD syndrome treatments.
Statistics for CANOMAD syndrome
CANOMAD syndrome: Broader Related Topics
Types of CANOMAD syndrome
User Interactive Forums
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Definitions of CANOMAD syndrome:
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list CANOMAD syndrome as a "rare disease".
Source - Orphanet
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