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Familial hyperchylomicronemia

Familial hyperchylomicronemia: Introduction

Familial hyperchylomicronemia: A rare inherited inborn error of metabolism involving the absence of the enzyme called lipoprotein lipase which results in increased blood triglyeride and chylomicron levels. More detailed information about the symptoms, causes, and treatments of Familial hyperchylomicronemia is available below.

Symptoms of Familial hyperchylomicronemia

Home Diagnostic Testing

Home medical testing related to Familial hyperchylomicronemia:

Wrongly Diagnosed with Familial hyperchylomicronemia?

Familial hyperchylomicronemia: Related Patient Stories

Causes of Familial hyperchylomicronemia

Read more about causes of Familial hyperchylomicronemia.

Disease Topics Related To Familial hyperchylomicronemia

Research the causes of these diseases that are similar to, or related to, Familial hyperchylomicronemia:

Misdiagnosis and Familial hyperchylomicronemia

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Familial hyperchylomicronemia: Research Doctors & Specialists

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Evidence Based Medicine Research for Familial hyperchylomicronemia

Medical research articles related to Familial hyperchylomicronemia include:

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Familial hyperchylomicronemia: Animations

Research about Familial hyperchylomicronemia

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Statistics for Familial hyperchylomicronemia

Familial hyperchylomicronemia: Broader Related Topics

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Definitions of Familial hyperchylomicronemia:

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

 

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