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WHIM syndrome

WHIM syndrome: Introduction

WHIM syndrome: A rare syndrome characterized by warts, hypogammaglobulinemia (low blood gammaglobulin levels), recurring bacterial infections and myelokathexis (form of neutropenia). It is a form of immunodeficiency disease caused by a mutation in a chemokine receptor. More detailed information about the symptoms, causes, and treatments of WHIM syndrome is available below.

Symptoms of WHIM syndrome

Home Diagnostic Testing

Home medical testing related to WHIM syndrome:

Wrongly Diagnosed with WHIM syndrome?

WHIM syndrome: Related Patient Stories

WHIM syndrome: Deaths

Read more about Deaths and WHIM syndrome.

WHIM syndrome: Complications

Read more about complications of WHIM syndrome.

Causes of WHIM syndrome

Read more about causes of WHIM syndrome.

Disease Topics Related To WHIM syndrome

Research the causes of these diseases that are similar to, or related to, WHIM syndrome:

Misdiagnosis and WHIM syndrome

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WHIM syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for WHIM syndrome

Medical research articles related to WHIM syndrome include:

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

WHIM syndrome: Animations

Research about WHIM syndrome

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

Statistics for WHIM syndrome

WHIM syndrome: Broader Related Topics

User Interactive Forums

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

Definitions of WHIM syndrome:

WHIM syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that WHIM syndrome, or a subtype of WHIM syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


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