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Pelger-Huet anomaly

Pelger-Huet anomaly: Introduction

Pelger-Huet anomaly: A rare blood disorder characterized by abnormal neutrophils which is a type of white blood cell. The condition can be inherited or result from bone marrow disorders. More detailed information about the symptoms, causes, and treatments of Pelger-Huet anomaly is available below.

Symptoms of Pelger-Huet anomaly

Home Diagnostic Testing

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Wrongly Diagnosed with Pelger-Huet anomaly?

Pelger-Huet anomaly: Related Patient Stories

Pelger-Huet anomaly: Complications

Read more about complications of Pelger-Huet anomaly.

Causes of Pelger-Huet anomaly

Read more about causes of Pelger-Huet anomaly.

Disease Topics Related To Pelger-Huet anomaly

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Misdiagnosis and Pelger-Huet anomaly

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Pelger-Huet anomaly: Research Doctors & Specialists

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Evidence Based Medicine Research for Pelger-Huet anomaly

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Pelger-Huet anomaly: Animations

Prognosis for Pelger-Huet anomaly

Prognosis for Pelger-Huet anomaly: harmless condition

Research about Pelger-Huet anomaly

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Statistics for Pelger-Huet anomaly

Pelger-Huet anomaly: Broader Related Topics

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Definitions of Pelger-Huet anomaly:

An inherited defect interfering with normal nuclear lobulation of neutrophils and eosinophils. The nuclei appear rodlike, spherical, or dumbbell-shaped and their structure is coarse and lumpy. (From Dorland, 27th ed) - (Source - Diseases Database)

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

 

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