ICF syndrome
ICF syndrome: Introduction
ICF syndrome: A very rare, recessively inherited syndrome characterized mainly by a weak immune system and facial anomalies.
More detailed information about the symptoms,
causes, and treatments of ICF syndrome is available below.
Symptoms of ICF syndrome
See full list of 23
symptoms of ICF syndrome
ICF syndrome: Complications
Read more about complications of ICF syndrome.
Medical Textbooks Online about ICF syndrome
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Less Common Symptoms of ICF syndrome
Read more about symptoms of ICF syndrome
Wrongly Diagnosed with ICF syndrome?
Causes of ICF syndrome
See full list of 62
causes of ICF syndrome
Read more about causes of ICF syndrome.
More information about causes of ICF syndrome:
Treatments for ICF syndrome
Read more about treatments for ICF syndrome
Evidence Based Medicine Research for ICF syndrome
Medical research articles related to ICF syndrome include:
Click here to find more evidence-based articles on the TRIP Database
Videos for ICF syndrome
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See full list of 5 related videos
Reseach about ICF syndrome
Visit our research pages for current research about ICF syndrome treatments.
Prevention of ICF syndrome
Prevention information for ICF syndrome has been compiled from various data sources
and may be inaccurate or incomplete.
None of these methods guarantee prevention of ICF syndrome.
Read more about prevention of ICF syndrome
User Interactive Forums
Read about other experiences, ask a question about ICF syndrome, or answer someone else's question, on our message boards:
Definitions of ICF syndrome:
Variable immunodeficiency with centromeric instability of chromosomes 1, 9, 16 and, less frequently, chromosome 2. Manifestations vary and most common symptoms include facial dysmorphism, mental retardation and prolonged respiratory, cutaneous, and gastrointestinal infections.
- (Source - Diseases Database)
ICF syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that ICF syndrome, or a subtype of ICF 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 ICF syndrome as a "rare disease".
Source - Orphanet
Contents for ICF syndrome:
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