CACH syndrome: Introduction
CACH syndrome: A rare syndrome characterized mainly by childhood ataxia and reduced myelination of the cerebral nerves. Motor and mental development in the first few years of life is normal with progressive neurodegeneration occurring between 2 and 5 years of age. Fever and trauma to the head can speed up disease progression.
More detailed information about the symptoms,
causes, and treatments of CACH syndrome is available below.
Symptoms of CACH syndrome
See full list of 11
symptoms of CACH syndrome
Home Diagnostic Testing
Home medical testing related to CACH syndrome:
- Nerve Neuropathy: Related Home Testing:
Wrongly Diagnosed with CACH syndrome?
CACH syndrome: Related Patient Stories
Causes of CACH syndrome
Read more about causes of CACH syndrome.
CACH syndrome: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and CACH syndrome
Undiagnosed stroke leads to misdiagnosed aphasia: BBC News UK reported on a man who
had been institutionalized and treated for mental illness
because he suffered from sudden...read more »
Dementia may be a drug interaction: A common scenario in aged care is for
a patient to show mental decline to dementia.
Whereas this can, of course, occur due to various medical conditions,
such as a...read more »
Mild traumatic brain injury often remains undiagnosed: Although the symptoms
of severe brain injury are hard to miss,
it is less clear for milder injuries,...read more »
MTBI misdiagnosed as balance problem: When a person has symptoms
such as vertigo or dizziness, a diagnosis of brain injury may go overlooked.
This is particularly true of mild traumatic brain injury (MTBI),...read more »
Brain pressure condition often misdiagnosed as dementia: A condition
that results from an excessive pressure of CSF within the brain is often...read more »
Post-concussive brain injury often misdiagnosed: A study found that soldiers who had
suffered a concussive injury in battle often were misdiagnosed on their return.
A variety of symptoms can...read more »
Children with migraine often misdiagnosed: A migraine often fails to be
correctly diagnosed in pediatric patients.
These patients are not the typical migraine sufferers, but migraines can also occur in children....read more »
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...read more »
Read more about Misdiagnosis and CACH syndrome
CACH syndrome: Research Doctors & Specialists
Research related physicians and medical specialists:
- Nerve Specialists:
- Neurology (Brain/CNS Specialists):
- Stroke & Vascular Specialists:
- more specialists...»
Other doctor, physician and specialist research services:
CACH syndrome: Rare Types
Rare types of diseases and disorders in related medical categories:
Evidence Based Medicine Research for CACH syndrome
Medical research articles related to CACH syndrome include:
Click here to find more evidence-based articles on the TRIP Database
CACH syndrome: Animations
More CACH syndrome animations & videos
Prognosis for CACH syndrome
Prognosis for CACH syndrome:
death tends to occur 5-10 years after symptoms start
More about prognosis of CACH syndrome
Research about CACH syndrome
Visit our research pages for current research about CACH syndrome treatments.
Statistics for CACH syndrome
CACH syndrome: Broader Related Topics
Types of CACH syndrome
User Interactive Forums
Read about other experiences, ask a question about CACH syndrome, or answer someone else's question, on our message boards:
Definitions of CACH syndrome:
CACH syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that CACH syndrome, or a subtype of CACH syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list CACH syndrome as a "rare disease".
Source - Orphanet
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