Cri-du-chat syndrome: Introduction
Cri-du-chat syndrome: A rare genetic disorder where a small portion of the short arm (p) of chromosome 5 is missing. The condition is characterized by a high-pitched cry which is similar to a cat's cry.
More detailed information about the symptoms,
causes, and treatments of Cri-du-chat syndrome is available below.
Symptoms of Cri-du-chat syndrome
See full list of 31
symptoms of Cri-du-chat syndrome
Home Diagnostic Testing
Home medical testing related to Cri-du-chat syndrome:
- Child Behavior: Home Testing
- Child General Health: Home Testing
Wrongly Diagnosed with Cri-du-chat syndrome?
Cri-du-chat syndrome: Related Patient Stories
Cri-du-chat syndrome: Complications
Read more about complications of Cri-du-chat syndrome.
Causes of Cri-du-chat syndrome
Read more about causes of Cri-du-chat syndrome.
Disease Topics Related To Cri-du-chat syndrome
Research the causes of these diseases that are similar to, or related to, Cri-du-chat syndrome:
Less Common Symptoms of Cri-du-chat syndrome
See full list of 18
occasional symptoms of Cri-du-chat syndrome
Cri-du-chat syndrome: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
- Vision & Eye: serious diseases often undiagnosed:
- Child Health Disorders -- serious medical disorders that may be undiagnosed:
- more undiagnosed conditions...»
Misdiagnosis and Cri-du-chat syndrome
Mild worm infections undiagnosed in children: Human worm infestations, esp. threadworm, can be overlooked in some cases,
because it may cause only mild...read more »
Mesenteric adenitis misdiagnosed as appendicitis in children: Because appendicitis is one of the
more feared conditions for a child with abdominal pain, it can be over...read more »
Blood pressure cuffs misdiagnose hypertension in children: One known misdiagnosis issue
with hyperension, arises in relation to the simple equipment used to test blood pressure.
The "cuff" around the arm to measure blood pressure can simply...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.
See misdiagnosis...read more »
Read more about Misdiagnosis and Cri-du-chat syndrome
Cri-du-chat syndrome: Research Doctors & Specialists
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
Hospitals & Clinics: Cri-du-chat syndrome
Research quality ratings and patient safety measures
for medical facilities in specialties related to Cri-du-chat syndrome:
Hospital & Clinic quality ratings »
Choosing the Best Hospital:
More general information, not necessarily in relation to Cri-du-chat syndrome,
on hospital performance and surgical care quality:
Evidence Based Medicine Research for Cri-du-chat syndrome
Medical research articles related to Cri-du-chat syndrome include:
Click here to find more evidence-based articles on the TRIP Database
Cri-du-chat syndrome: Animations
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Research about Cri-du-chat syndrome
Visit our research pages for current research about Cri-du-chat syndrome treatments.
Statistics for Cri-du-chat syndrome
Cri-du-chat syndrome: Broader Related Topics
Types of Cri-du-chat syndrome
Cri-du-chat syndrome Message Boards
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User Interactive Forums
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Definitions of Cri-du-chat syndrome:
Deletion of the short arm of chromosome 5 characterized by a variable clinical picture consisting of severe mental deficiency, growth retardation, multiple abnormalities and a peculiar crying sound resembling that of a suffering kitten (hence the synonym crying cat syndrome or cri du chat syndrome), that disappears within weeks or months after birth.
- (Source - Diseases Database)
Cri-du-chat syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Cri-du-chat syndrome, or a subtype of Cri-du-chat 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 Cri-du-chat syndrome as a "rare disease".
Source - Orphanet
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