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Diseases » ICF syndrome » Introduction
 

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

Medical Books Excerpts
 

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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