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Diseases » Omenn syndrome » Introduction
 

Omenn syndrome

Omenn syndrome: Introduction

Omenn syndrome: A rare inherited disorder of the immune system involving B and T lymphocytes and characterized by skin rash and frequent infections. More detailed information about the symptoms, causes, and treatments of Omenn syndrome is available below.

Symptoms of Omenn syndrome

See full list of 13 symptoms of Omenn syndrome

Omenn syndrome: Complications

Review possible medical complications related to Omenn syndrome:

Medical Textbooks Online about Omenn syndrome

Medical Books Excerpts
 

Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Wrongly Diagnosed with Omenn syndrome?

Causes of Omenn syndrome

Read more about causes of Omenn syndrome.

Evidence Based Medicine Research for Omenn syndrome

Medical research articles related to Omenn syndrome include:

Click here to find more evidence-based articles on the TRIP Database

Videos for Omenn syndrome

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Prognosis for Omenn syndrome

Prognosis for Omenn syndrome: poor

More about prognosis of Omenn syndrome

Reseach about Omenn syndrome

Visit our research pages for current research about Omenn syndrome treatments.

User Interactive Forums

Read about other experiences, ask a question about Omenn syndrome, or answer someone else's question, on our message boards:

Definitions of Omenn syndrome:

Omenn syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Omenn syndrome, or a subtype of Omenn 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 Omenn syndrome as a "rare disease".
Source - Orphanet


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